A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891039



Internal ID22666071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87401751..87404794hg38UCSC Ensembl
chr6:88111469..88114512hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383044
hg193044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891039
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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