A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556929



Internal ID16344338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:758819..763196hg38UCSC Ensembl
Innerchr12:867985..872362hg19UCSC Ensembl
Innerchr12:738246..742623hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg384378
hg194378
hg184378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2258n54
Supporting Variantsnssv786109, nssv786110
Samples
Known GenesWNK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556929
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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