A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519035



Internal ID18470630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38754726..38961204hg38UCSC Ensembl
Innerchr11:38776276..38982754hg19UCSC Ensembl
Innerchr11:38732852..38939330hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38206479
hg19206479
hg18206479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052196
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)nssv3519035
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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