A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584815



Internal ID16372224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240629912..240654527hg38UCSC Ensembl
Innerchr2:241569329..241593944hg19UCSC Ensembl
Innerchr2:241218002..241242617hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3824616
hg1924616
hg1824616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151191
SamplesHGDP00407
Known GenesGPR35
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584815
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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