A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034376



Internal ID19123598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140523183..140660429hg38UCSC Ensembl
Innerchr6:140844320..140981566hg19UCSC Ensembl
Innerchr6:140886013..141023259hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38137247
hg19137247
hg18137247
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654436, nssv3654437
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)nsv1034376
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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