A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv788037



Internal ID15735307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10428209..10444437hg38UCSC Ensembl
Innerchr12:10580808..10597036hg19UCSC Ensembl
Innerchr12:10472075..10488303hg18UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3816229
hg1916229
hg1816229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557471
Supporting Variants
Samples
Known GenesKLRC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv788037
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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