A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3645821



Internal ID18944102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101420320..101486554hg38UCSC Ensembl
Innerchr5:100756024..100822258hg19UCSC Ensembl
Innerchr5:100783923..100850157hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3866235
hg1966235
hg1866235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024075
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)nssv3645821
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