A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580919



Internal ID16368328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9304549..9306151hg38UCSC Ensembl
Innerchr2:9444678..9446280hg19UCSC Ensembl
Innerchr2:9362129..9363731hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381603
hg191603
hg181603
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv903585, nssv903584, nssv903586, nssv903587
Samples
Known GenesASAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580919
Frequency
Sample Size17421
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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