A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140870



Internal ID340064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16966207..16966464hg38UCSC Ensembl
chr5:16966316..16966573hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962127
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140870
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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