A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242181



Internal ID21306010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178682974..178686162hg38UCSC Ensembl
Outerchr5:178680821..178691854hg38UCSC Ensembl
Innerchr5:178109975..178113163hg19UCSC Ensembl
Outerchr5:178107822..178118855hg19UCSC Ensembl
Innerchr5:178042581..178045769hg18UCSC Ensembl
Outerchr5:178040428..178051461hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3811034
hg1911034
hg1811034
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170024
Supporting Variants
SamplesNGO_24
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14242181
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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