A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576930



Internal ID18875211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:6093014..6126364hg38UCSC Ensembl
Innerchr2:6233146..6266496hg19UCSC Ensembl
Innerchr2:6150597..6183947hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3833351
hg1933351
hg1833351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003786
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3576930
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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