A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697171



Internal ID15433823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12419940..12429304hg38UCSC Ensembl
Innerchr16:12513797..12523161hg19UCSC Ensembl
Innerchr16:12421298..12430662hg18UCSC Ensembl
Innerchr16:12421298..12430662hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg389365
hg199365
hg189365
hg179365
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520000
Supporting Variants
Samples
Known GenesSNX29
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697171
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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