A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584055



Internal ID16371464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:188402096..188628959hg38UCSC Ensembl
Innerchr2:189266823..189493686hg19UCSC Ensembl
Innerchr2:188975068..189201931hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38226864
hg19226864
hg18226864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv928423
Samples
Known GenesGULP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584055
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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