A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034677



Internal ID19123898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85764650..85856745hg38UCSC Ensembl
Innerchr6:86474368..86566463hg19UCSC Ensembl
Innerchr6:86531087..86623182hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3892096
hg1992096
hg1892096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6079n100
Supporting Variantsnssv3648902
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)nsv1034677
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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