A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031707



Internal ID19120929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106355450..106448775hg38UCSC Ensembl
Innerchr6:106803325..106896650hg19UCSC Ensembl
Innerchr6:106910018..107003343hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3893326
hg1993326
hg1893326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654278
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)nsv1031707
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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