A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904995



Internal ID15852265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:33540295..33541741hg38UCSC Ensembl
Innerchr2:33765362..33766808hg19UCSC Ensembl
Innerchr2:33618866..33620312hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg381447
hg191447
hg181447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581324
Supporting Variants
Samples
Known GenesRASGRP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv904995
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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