A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026686



Internal ID19115904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76726430..76751356hg38UCSC Ensembl
Innerchr6:77436147..77461073hg19UCSC Ensembl
Innerchr6:77492866..77517792hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3824927
hg1924927
hg1824927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6021n100
Supporting Variantsnssv3658864, nssv3658866, nssv3658867, nssv3658865
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)nsv1026686
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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