A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032949



Internal ID19122171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:14640318..14653295hg38UCSC Ensembl
Innerchr6:14640549..14653526hg19UCSC Ensembl
Innerchr6:14748528..14761505hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3812978
hg1912978
hg1812978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654792
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)nsv1032949
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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