A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916270



Internal ID22691489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69323896..69323951hg38UCSC Ensembl
chr8:70236131..70236186hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435407
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916270
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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