A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654295



Internal ID18952576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110075473..110099518hg38UCSC Ensembl
Innerchr6:110396676..110420721hg19UCSC Ensembl
Innerchr6:110503369..110527414hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3824046
hg1924046
hg1824046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026085
Supporting Variants
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)nssv3654295
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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