A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710078



Internal ID18661673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34620051..34767784hg38UCSC Ensembl
Innerchr11:34641598..34789331hg19UCSC Ensembl
Innerchr11:34598174..34745907hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38147734
hg19147734
hg18147734
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051492
Supporting Variants
Samples
Known GenesEHF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710078
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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