A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582786



Internal ID16023509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:120338344..120352811hg38UCSC Ensembl
Innerchr2:121095920..121110387hg19UCSC Ensembl
Innerchr2:120812390..120826857hg18UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg3814468
hg1914468
hg1814468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv916430
Samples
Known GenesINHBB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582786
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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