A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150705



Internal ID15873580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4801226..4845976hg38UCSC Ensembl
Innerchr2:4848816..4893566hg19UCSC Ensembl
Innerchr2:4826691..4871441hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3844751
hg1944751
hg1844751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580863
Supporting Variants
SamplesHGDP00251
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150705
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