A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648206



Internal ID18599801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:155479846..155510105hg38UCSC Ensembl
Innerchr5:154859406..154889665hg19UCSC Ensembl
Innerchr5:154839599..154869858hg18UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3830260
hg1930260
hg1830260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032678
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)nssv3648206
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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