A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692963



Internal ID15082929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70660097..70770840hg38UCSC Ensembl
Innerchr16:70694000..70804743hg19UCSC Ensembl
Innerchr16:69251501..69362244hg18UCSC Ensembl
Innerchr16:69251501..69362244hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38110744
hg19110744
hg18110744
hg17110744
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517391
Supporting Variants
Samples
Known GenesIL34, MTSS1L, VAC14, VAC14-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692963
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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