A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv798872



Internal ID16092828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:78085837..78118961hg38UCSC Ensembl
Innerchr12:78479617..78512741hg19UCSC Ensembl
Innerchr12:77003748..77036872hg18UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3833125
hg1933125
hg1833125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559434
Supporting Variants
Samples
Known GenesNAV3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv798872
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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