A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997566



Internal ID19157102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109829526..109876232hg38UCSC Ensembl
Innerchr1:110372148..110418854hg19UCSC Ensembl
Innerchr1:110173671..110220377hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3846707
hg1946707
hg1846707
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3484210
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)nsv997566
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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