A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016185



Internal ID19105404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:86788057..86848056hg38UCSC Ensembl
Innerchr6:87497775..87557774hg19UCSC Ensembl
Innerchr6:87554494..87614493hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3860000
hg1960000
hg1860000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648938
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)nsv1016185
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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