A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019246



Internal ID19108464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10484803..10624983hg38UCSC Ensembl
Innerchr7:10524430..10664610hg19UCSC Ensembl
Innerchr7:10490955..10631135hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38140181
hg19140181
hg18140181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752882
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019246
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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