A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705646



Internal ID15442298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12128207..12141020hg38UCSC Ensembl
Innerchr16:12222064..12234877hg19UCSC Ensembl
Innerchr16:12129565..12142378hg18UCSC Ensembl
Innerchr16:12129565..12142378hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3812814
hg1912814
hg1812814
hg1712814
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528952
Supporting Variants
Samples
Known GenesSNX29
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705646
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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