A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515894



Internal ID15442951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66083757..66104680hg38UCSC Ensembl
Innerchr4:66949475..66970398hg19UCSC Ensembl
Innerchr4:66632070..66652993hg18UCSC Ensembl
Innerchr4:66778241..66799164hg17UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3820924
hg1920924
hg1820924
hg1720924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv680891, nssv686186, nssv692036, nssv688211, nssv671403, nssv672189, nssv655090, nssv670489, nssv657425, nssv665178, nssv667580, nssv686648, nssv663081, nssv678200, nssv684056, nssv675675, nssv679860
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515894
Frequency
Sample Size2026
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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