A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698964



Internal ID15088930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57753115..57786197hg38UCSC Ensembl
Innerchr16:57787027..57820109hg19UCSC Ensembl
Innerchr16:56344528..56377610hg18UCSC Ensembl
Innerchr16:56344528..56377610hg17UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3833083
hg1933083
hg1833083
hg1733083
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523237
Supporting Variants
Samples
Known GenesKATNB1, KIFC3, MIR6772
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698964
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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