A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900123



Internal ID22675262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131323396..131328836hg38UCSC Ensembl
chr6:131644536..131649976hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg385441
hg195441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423447
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900123
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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