A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv906859



Internal ID16200815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:36459968..36488546hg38UCSC Ensembl
Innerchr2:36687111..36715689hg19UCSC Ensembl
Innerchr2:36540615..36569193hg18UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3828579
hg1928579
hg1828579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581468
Supporting Variants
Samples
Known GenesCRIM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv906859
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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