A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3646934



Internal ID18945215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106530161..106770824hg38UCSC Ensembl
Innerchr5:105865862..106106525hg19UCSC Ensembl
Innerchr5:105893761..106134424hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38240664
hg19240664
hg18240664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021423
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)nssv3646934
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