A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556922



Internal ID15997645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:758140..764839hg38UCSC Ensembl
Innerchr12:867306..874005hg19UCSC Ensembl
Innerchr12:737567..744266hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg386700
hg196700
hg186700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2259n54
Supporting Variantsnssv786085, nssv786083, nssv786084, nssv786089, nssv786092, nssv786087, nssv786086, nssv786088, nssv786091, nssv786090
Samples
Known GenesWNK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556922
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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