A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655592



Internal ID18953873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65212670..65697197hg38UCSC Ensembl
Innerchr7:64673048..65162170hg19UCSC Ensembl
Innerchr7:64310483..64799605hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38484528
hg19489123
hg18489123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016478
Supporting Variants
Samples
Known GenesINTS4L2, LOC441242, ZNF92
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655592
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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