A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580924



Internal ID16368333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9305072..9306151hg38UCSC Ensembl
Innerchr2:9445201..9446280hg19UCSC Ensembl
Innerchr2:9362652..9363731hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381080
hg191080
hg181080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv903593, nssv903592
Samples
Known GenesASAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580924
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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