A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032896



Internal ID19122118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:81700080..81726888hg38UCSC Ensembl
Innerchr6:82409797..82436605hg19UCSC Ensembl
Innerchr6:82466516..82493324hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3826809
hg1926809
hg1826809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6076n100
Supporting Variantsnssv3648874
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)nsv1032896
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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