A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705622



Internal ID15095588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89199455..89273708hg38UCSC Ensembl
Innerchr7:88828769..88903022hg19UCSC Ensembl
Innerchr7:88666705..88740958hg18UCSC Ensembl
Innerchr7:88473420..88547673hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3874254
hg1974254
hg1874254
hg1774254
Variant TypeCNV gain
Copy Number
Allele State
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)nssv705622
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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