A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv903582



Internal ID16197538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9304549..9305898hg38UCSC Ensembl
Innerchr2:9444678..9446027hg19UCSC Ensembl
Innerchr2:9362129..9363478hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381350
hg191350
hg181350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580917
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)nssv903582
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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