A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3727990



Internal ID18679585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:25776182..25842245hg38UCSC Ensembl
Innerchr2:25999051..26065114hg19UCSC Ensembl
Innerchr2:25852555..25918618hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3866064
hg1966064
hg1866064
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000297
Supporting Variants
Samples
Known GenesASXL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3727990
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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