A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905013



Internal ID22680193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138735502..138735859hg38UCSC Ensembl
chr6:139056639..139056996hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416798
Samples
Known GenesLOC100507462
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905013
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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