A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655213



Internal ID18606808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89018127..89040085hg38UCSC Ensembl
Innerchr7:88647441..88669399hg19UCSC Ensembl
Innerchr7:88485377..88507335hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3821959
hg1921959
hg1821959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025214
Supporting Variants
Samples
Known GenesZNF804B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655213
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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