A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018662



Internal ID19107879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83429511..83589975hg38UCSC Ensembl
Innerchr7:83058827..83219291hg19UCSC Ensembl
Innerchr7:82896763..83057227hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38160465
hg19160465
hg18160465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755419
Samples
Known GenesSEMA3E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018662
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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