A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3728893



Internal ID19027174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88833599..88878438hg38UCSC Ensembl
Innerchr2:89133112..89177954hg19UCSC Ensembl
Innerchr2:88914227..88959069hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3844840
hg1944843
hg1844843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013685
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)nssv3728893
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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