A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170137



Internal ID21314198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179668592..179681642hg38UCSC Ensembl
Outerchr5:179659493..179683849hg38UCSC Ensembl
Innerchr5:179095593..179108643hg19UCSC Ensembl
Outerchr5:179086494..179110850hg19UCSC Ensembl
Innerchr5:179028199..179041249hg18UCSC Ensembl
Outerchr5:179019100..179043456hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3824357
hg1924357
hg1824357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247784
SamplesNGO_24
Known GenesCBY3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170137
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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