A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3571274



Internal ID18522869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:1416577..1519167hg38UCSC Ensembl
Innerchr2:1420349..1522939hg19UCSC Ensembl
Innerchr2:1399356..1501946hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38102591
hg19102591
hg18102591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997857
Supporting Variants
Samples
Known GenesTPO
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3571274
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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