A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695122



Internal ID15085088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8677329..8683260hg38UCSC Ensembl
Innerchr16:8771186..8777117hg19UCSC Ensembl
Innerchr16:8678687..8684618hg18UCSC Ensembl
Innerchr16:8678687..8684618hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg385932
hg195932
hg185932
hg175932
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522342
Supporting Variants
Samples
Known GenesABAT
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695122
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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