A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169524



Internal ID21313757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41587169..41595002hg38UCSC Ensembl
Outerchr5:41583900..41599347hg38UCSC Ensembl
Innerchr5:41587271..41595104hg19UCSC Ensembl
Outerchr5:41584002..41599449hg19UCSC Ensembl
Innerchr5:41623028..41630861hg18UCSC Ensembl
Outerchr5:41619759..41635206hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3815448
hg1915448
hg1815448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247785
SamplesNGO_41
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169524
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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