A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580458



Internal ID18878739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89928002..90082579hg38UCSC Ensembl
Innerchr2:89966812..90121421hg19UCSC Ensembl
Innerchr2:89604119..89758726hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38154578
hg19154610
hg18154608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006742
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)nssv3580458
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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