A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580918



Internal ID16368327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9304549..9306011hg38UCSC Ensembl
Innerchr2:9444678..9446140hg19UCSC Ensembl
Innerchr2:9362129..9363591hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381463
hg191463
hg181463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6683n54
Supporting Variantsnssv903583
Samples
Known GenesASAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580918
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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