A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635900



Internal ID18934181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18825665..18949411hg38UCSC Ensembl
Innerchr5:18825774..18949520hg19UCSC Ensembl
Innerchr5:18861531..18985277hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38123747
hg19123747
hg18123747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027738
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)nssv3635900
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