A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150665



Internal ID15872757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:2598626..2621476hg38UCSC Ensembl
Innerchr2:2602398..2625248hg19UCSC Ensembl
Innerchr2:2581405..2604255hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3822851
hg1922851
hg1822851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580769
Supporting Variants
SamplesHGDP00031
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150665
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