A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729291



Internal ID19027572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:184091387..184451937hg38UCSC Ensembl
Innerchr2:184956114..185316664hg19UCSC Ensembl
Innerchr2:184664359..185024909hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38360551
hg19360551
hg18360551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012174
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3729291
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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