A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016156



Internal ID19105374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80568256..80584685hg38UCSC Ensembl
Innerchr6:81277973..81294402hg19UCSC Ensembl
Innerchr6:81334692..81351121hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3816430
hg1916430
hg1816430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6073n100
Supporting Variantsnssv3750109, nssv3648840
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)nsv1016156
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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