A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004402



Internal ID19093620
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 StatusM
Merged Variantsdgv3718n100
Supporting Variantsnssv3577035
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)nsv1004402
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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