A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006396



Internal ID19095613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:64258020..64303802hg38UCSC Ensembl
Innerchr1:64723703..64769485hg19UCSC Ensembl
Innerchr1:64496291..64542073hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3845783
hg1945783
hg1845783
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3701243
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)nsv1006396
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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