A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895095



Internal ID22670172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:86921043..86926615hg38UCSC Ensembl
chr6:87630761..87636333hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg385573
hg195573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439202
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895095
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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