A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635959



Internal ID18934240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25933573..25998816hg38UCSC Ensembl
Innerchr5:25933682..25998925hg19UCSC Ensembl
Innerchr5:25969439..26034682hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3865244
hg1965244
hg1865244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022260
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)nssv3635959
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