A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648126



Internal ID18946407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:135707843..135730733hg38UCSC Ensembl
Innerchr5:135043532..135066422hg19UCSC Ensembl
Innerchr5:135071431..135094321hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3822891
hg1922891
hg1822891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017948
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)nssv3648126
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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