A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899575



Internal ID22674706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:86207262..86280735hg38UCSC Ensembl
chr6:86916980..86990453hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3873474
hg1973474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899575
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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