A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031005



Internal ID19120226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:9821885..9888057hg38UCSC Ensembl
Innerchr6:9822118..9888290hg19UCSC Ensembl
Innerchr6:9930104..9996276hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3866173
hg1966173
hg1866173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654761
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)nsv1031005
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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