A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv902055



Internal ID16196011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:309480..391781hg38UCSC Ensembl
Innerchr2:309480..391781hg19UCSC Ensembl
Innerchr2:299480..381781hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3882302
hg1982302
hg1882302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580424
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv902055
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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