A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022847



Internal ID19112065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:69590629..69628007hg38UCSC Ensembl
Innerchr6:70300521..70337899hg19UCSC Ensembl
Innerchr6:70357242..70394620hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3837379
hg1937379
hg1837379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3658804
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)nsv1022847
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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