A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170107



Internal ID21314168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:161114181..161122691hg38UCSC Ensembl
Outerchr5:161112752..161125519hg38UCSC Ensembl
Innerchr5:160541188..160549698hg19UCSC Ensembl
Outerchr5:160539759..160552526hg19UCSC Ensembl
Innerchr5:160473766..160482276hg18UCSC Ensembl
Outerchr5:160472337..160485104hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3812768
hg1912768
hg1812768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247516
SamplesPML_3
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170107
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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