A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583667



Internal ID16024390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:174410951..174466210hg38UCSC Ensembl
Innerchr2:175275679..175330938hg19UCSC Ensembl
Innerchr2:174983925..175039184hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3855260
hg1955260
hg1855260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv925610
Samples
Known GenesGPR155, SCRN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583667
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer