A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584900



Internal ID16372309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240923534..240928657hg38UCSC Ensembl
Innerchr2:241862951..241868074hg19UCSC Ensembl
Innerchr2:241511624..241516747hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg385124
hg195124
hg185124
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7381n54
Supporting Variantsnssv934423, nssv934422
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584900
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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