A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3577035



Internal ID18875316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13062529..13135754hg38UCSC Ensembl
Innerchr2:13202654..13275879hg19UCSC Ensembl
Innerchr2:13120105..13193330hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3873226
hg1973226
hg1873226
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004402
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)nssv3577035
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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