A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011574



Internal ID19100791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34434857..34515960hg38UCSC Ensembl
Innerchr2:34659924..34741027hg19UCSC Ensembl
Innerchr2:34513428..34594531hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3881104
hg1981104
hg1881104
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3758n100
Supporting Variantsnssv3580990, nssv3728048, nssv3580992, nssv3580991
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)nsv1011574
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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