A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016478



Internal ID19105697
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 StatusM
Merged Variantsdgv6435n100
Supporting Variantsnssv3655593, nssv3655592
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)nsv1016478
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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