A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656682



Internal ID15046648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89275360..89275463hg38UCSC Ensembl
Innerchr7:88904674..88904777hg19UCSC Ensembl
Innerchr7:88742610..88742713hg18UCSC Ensembl
Innerchr7:88549325..88549428hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38104
hg19104
hg18104
hg17104
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515995
Supporting Variants
Samples
Known GenesZNF804B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656682
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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