A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648201



Internal ID18599796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:155474295..155509336hg38UCSC Ensembl
Innerchr5:154853855..154888896hg19UCSC Ensembl
Innerchr5:154834048..154869089hg18UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3835042
hg1935042
hg1835042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033393
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)nssv3648201
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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