A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3645914



Internal ID18944195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:103700839..103751376hg38UCSC Ensembl
Innerchr5:103036540..103087077hg19UCSC Ensembl
Innerchr5:103064439..103114976hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3850538
hg1950538
hg1850538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028217
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)nssv3645914
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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