A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556909



Internal ID16344318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:757691..761617hg38UCSC Ensembl
Innerchr12:866857..870783hg19UCSC Ensembl
Innerchr12:737118..741044hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg383927
hg193927
hg183927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2257n54
Supporting Variantsnssv785893
Samples
Known GenesWNK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556909
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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