A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv785903



Internal ID15733173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:757691..763747hg38UCSC Ensembl
Innerchr12:866857..872913hg19UCSC Ensembl
Innerchr12:737118..743174hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg386057
hg196057
hg186057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556913
Supporting Variants
Samples
Known GenesWNK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv785903
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer