A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027824



Internal ID19117042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:47131890..47172621hg38UCSC Ensembl
Innerchr7:47171488..47212219hg19UCSC Ensembl
Innerchr7:47138013..47178744hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3840732
hg1940732
hg1840732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661241
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)nsv1027824
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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