A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729263



Internal ID18680858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:154738421..154923497hg38UCSC Ensembl
Innerchr2:155594933..155780009hg19UCSC Ensembl
Innerchr2:155303179..155488255hg18UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38185077
hg19185077
hg18185077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003775
Supporting Variants
Samples
Known GenesKCNJ3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3729263
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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