A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642158



Internal ID18940439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:58013204..58042530hg38UCSC Ensembl
Innerchr5:57309031..57338357hg19UCSC Ensembl
Innerchr5:57344788..57374114hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3829327
hg1929327
hg1829327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015769
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)nssv3642158
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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