A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015358



Internal ID19104575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77324279..77357154hg38UCSC Ensembl
Innerchr6:78033996..78066871hg19UCSC Ensembl
Innerchr6:78090715..78123590hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3832876
hg1932876
hg1832876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3659055
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)nsv1015358
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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