A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710112



Internal ID19008393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38301195..38340379hg38UCSC Ensembl
Innerchr11:38322745..38361929hg19UCSC Ensembl
Innerchr11:38279321..38318505hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3839185
hg1939185
hg1839185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039106
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)nssv3710112
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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