A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031116



Internal ID19120337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15388718..15528962hg38UCSC Ensembl
Innerchr7:15428343..15568587hg19UCSC Ensembl
Innerchr7:15394868..15535112hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38140245
hg19140245
hg18140245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643183
Samples
Known GenesAGMO
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031116
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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