A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3637092



Internal ID18935373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:37882324..37936250hg38UCSC Ensembl
Innerchr5:37882426..37936352hg19UCSC Ensembl
Innerchr5:37918183..37972109hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3853927
hg1953927
hg1853927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028115
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)nssv3637092
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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