A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749613



Internal ID18701208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163692949..163748995hg38UCSC Ensembl
Innerchr6:164113981..164170027hg19UCSC Ensembl
Innerchr6:164033971..164090017hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3856047
hg1956047
hg1856047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025171
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)nssv3749613
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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