A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139788



Internal ID338977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:117910367..117910599hg38UCSC Ensembl
chr3:117629214..117629446hg19UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16936542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139788
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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