A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3645889



Internal ID18944170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:102128569..102186521hg38UCSC Ensembl
Innerchr5:101464273..101522225hg19UCSC Ensembl
Innerchr5:101492172..101550124hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3857953
hg1957953
hg1857953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025308
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)nssv3645889
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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