A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv786065



Internal ID15733335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:757691..765362hg38UCSC Ensembl
Innerchr12:866857..874528hg19UCSC Ensembl
Innerchr12:737118..744789hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg387672
hg197672
hg187672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556917
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)nssv786065
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