A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582529



Internal ID16369938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:100071316..100137028hg38UCSC Ensembl
Innerchr2:100687778..100753490hg19UCSC Ensembl
Innerchr2:100054210..100119922hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3865713
hg1965713
hg1865713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151115
Samples1780862592_A
Known GenesAFF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582529
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer