A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3571281



Internal ID18522876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:1428027..1512593hg38UCSC Ensembl
Innerchr2:1431799..1516365hg19UCSC Ensembl
Innerchr2:1410806..1495372hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3884567
hg1984567
hg1884567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998563
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)nssv3571281
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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