A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517686



Internal ID15444979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:80009047..80023890hg38UCSC Ensembl
Innerchr17:77982846..77997689hg19UCSC Ensembl
Innerchr17:75597441..75612284hg18UCSC Ensembl
Innerchr17:75597441..75612284hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3814844
hg1914844
hg1814844
hg1714844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671473, nssv677529, nssv656435, nssv652837, nssv685294, nssv666873, nssv688262, nssv685094, nssv674437, nssv666648, nssv689505, nssv680933, nssv691480, nssv667087, nssv693164, nssv672921, nssv677867, nssv667524, nssv656396, nssv675932, nssv663523, nssv672898, nssv660734, nssv658932, nssv690399, nssv687581, nssv675726, nssv659532, nssv683616, nssv663212, nssv682596, nssv690446, nssv658671, nssv653024, nssv677919, nssv654320
Samples
Known GenesTBC1D16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517686
Frequency
Sample Size2026
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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