A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648195



Internal ID18599790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:155473737..155495081hg38UCSC Ensembl
Innerchr5:154853297..154874641hg19UCSC Ensembl
Innerchr5:154833490..154854834hg18UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3821345
hg1921345
hg1821345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032192
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)nssv3648195
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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