A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586979



Internal ID18538574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:239949097..239999118hg38UCSC Ensembl
Innerchr2:240888514..240938535hg19UCSC Ensembl
Innerchr2:240537187..240587208hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3850022
hg1950022
hg1850022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014414
Supporting Variants
Samples
Known GenesNDUFA10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3586979
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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