A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515885



Internal ID15442942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68525208..68539492hg38UCSC Ensembl
Innerchr6:69235100..69249384hg19UCSC Ensembl
Innerchr6:69291821..69306105hg18UCSC Ensembl
Innerchr6:69291821..69306105hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3814285
hg1914285
hg1814285
hg1714285
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689345, nssv652807, nssv666570, nssv664659, nssv660911, nssv669138, nssv677628, nssv657513, nssv679329, nssv666907, nssv680605, nssv677331, nssv691036, nssv658724, nssv693946, nssv658515, nssv663159, nssv668931, nssv658939, nssv667475, nssv652908, nssv683600, nssv691951, nssv675152, nssv684551, nssv679258, nssv671244, nssv664189, nssv690486, nssv681787, nssv670355, nssv671310, nssv698484, nssv689686, nssv670396, nssv684914, nssv663503, nssv693357, nssv662800, nssv668822, nssv660041, nssv678104, nssv680061, nssv693390, nssv665182, nssv680523, nssv680361, nssv675587, nssv685129, nssv677798, nssv669982, nssv659060, nssv692563, nssv680894, nssv689878, nssv687484, nssv686252, nssv665156, nssv704319, nssv668222, nssv671675, nssv688177, nssv688753, nssv679448, nssv662218, nssv675183, nssv691885, nssv652264, nssv681383, nssv654485, nssv660851, nssv692499, nssv666167, nssv667161, nssv686190, nssv683964, nssv673806, nssv656790
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515885
Frequency
Sample Size2026
Observed Gain26
Observed Loss52
Observed Complex0
Frequencyn/a


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