A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019180



Internal ID18761714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64869511..65052464hg38UCSC Ensembl
Innerchr7:64329889..64512842hg19UCSC Ensembl
Innerchr7:63967324..64150277hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38182954
hg19182954
hg18182954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655507
Samples
Known GenesCCT6P3, ERV3-1, ZNF117, ZNF273
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019180
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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