A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008699



Internal ID19097916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80484648..80542449hg38UCSC Ensembl
Innerchr1:80950333..81008134hg19UCSC Ensembl
Innerchr1:80722921..80780722hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3857802
hg1957802
hg1857802
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3482170
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)nsv1008699
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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