A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649856



Internal ID18948137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100643558..100699219hg38UCSC Ensembl
Innerchr6:101091434..101147095hg19UCSC Ensembl
Innerchr6:101198155..101253816hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3855662
hg1955662
hg1855662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032826
Supporting Variants
Samples
Known GenesASCC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3649856
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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