A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584455



Internal ID16025178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:216660520..216694012hg38UCSC Ensembl
Innerchr2:217525243..217558735hg19UCSC Ensembl
Innerchr2:217233488..217266980hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3833493
hg1933493
hg1833493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150822
SamplesHGDP00551
Known GenesIGFBP2, IGFBP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584455
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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