A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581830



Internal ID16369239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:49422030..49512223hg38UCSC Ensembl
Innerchr2:49649168..49739361hg19UCSC Ensembl
Innerchr2:49502672..49592865hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3890194
hg1990194
hg1890194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv908353
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581830
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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