A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556629



Internal ID16344038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134479021..134851577hg38UCSC Ensembl
Innerchr11:134348915..134721471hg19UCSC Ensembl
Innerchr11:133854125..134226681hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38372557
hg19372557
hg18372557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2207n54
Supporting Variantsnssv1176217, nssv1176219, nssv785173, nssv785170, nssv785171, nssv785172, nssv1176220, nssv1176218
Samples1780854445_A, NINDS_147, 1780862388_A, HGDP00671
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556629
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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