A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572361



Internal ID16359770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34939284..34962310hg38UCSC Ensembl
Innerchr16:34173678..34196681hg19UCSC Ensembl
Innerchr16:34031179..34054182hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3823027
hg1923004
hg1823004
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5081n54
Supporting Variantsnssv856213, nssv856214, nssv856225, nssv856224, nssv856228, nssv856227, nssv856219, nssv856229, nssv856211, nssv856217, nssv856223, nssv856210, nssv856221, nssv856218, nssv856226, nssv856215, nssv856222, nssv856220, nssv856216, nssv856212
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572361
Frequency
Sample Size17421
Observed Gain16
Observed Loss4
Observed Complex0
Frequencyn/a


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