A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556937



Internal ID15997660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:759098..765362hg38UCSC Ensembl
Innerchr12:868264..874528hg19UCSC Ensembl
Innerchr12:738525..744789hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg386265
hg196265
hg186265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2259n54
Supporting Variantsnssv786219, nssv786220
Samples
Known GenesWNK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556937
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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