A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5470633



Internal ID248387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110181184..110181260hg38UCSC Ensembl
chr6:110502387..110502463hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987946
Samples
Known GenesCDC40
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5470633
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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