A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015500



Internal ID19104717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:145067422..145100367hg38UCSC Ensembl
Innerchr6:145388558..145421503hg19UCSC Ensembl
Innerchr6:145430251..145463196hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3832946
hg1932946
hg1832946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654458
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)nsv1015500
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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