A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv902178



Internal ID16196134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:1519167..1616123hg38UCSC Ensembl
Innerchr2:1522939..1619895hg19UCSC Ensembl
Innerchr2:1501946..1598902hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3896957
hg1996957
hg1896957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580499
Supporting Variants
Samples
Known GenesTPO
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv902178
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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