A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053895



Internal ID18796426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132032553..132083280hg38UCSC Ensembl
Innerchr11:131902447..131953174hg19UCSC Ensembl
Innerchr11:131407657..131458384hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3850728
hg1950728
hg1850728
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710767
Samples
Known GenesNTM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053895
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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