A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv903580



Internal ID16197536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9304549..9305582hg38UCSC Ensembl
Innerchr2:9444678..9445711hg19UCSC Ensembl
Innerchr2:9362129..9363162hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381034
hg191034
hg181034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580916
Supporting Variants
Samples
Known GenesASAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv903580
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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