A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030970



Internal ID19120190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:102235243..102287407hg38UCSC Ensembl
Innerchr6:102683118..102735282hg19UCSC Ensembl
Innerchr6:102789811..102841975hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3852165
hg1952165
hg1852165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6114n100
Supporting Variantsnssv3649864
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)nsv1030970
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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