A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579140



Internal ID18530735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:30592120..30626477hg38UCSC Ensembl
Innerchr2:30814986..30849343hg19UCSC Ensembl
Innerchr2:30668490..30702847hg18UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg3834358
hg1934358
hg1834358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003432
Supporting Variants
Samples
Known GenesLCLAT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579140
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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