A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054175



Internal ID19143394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31556967..31688096hg38UCSC Ensembl
Innerchr11:31578514..31709644hg19UCSC Ensembl
Innerchr11:31535090..31666220hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38131130
hg19131131
hg18131131
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516567
Samples
Known GenesELP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054175
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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