A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914380



Internal ID22689597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91103277..91173398hg38UCSC Ensembl
chr8:92115505..92185626hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3870122
hg1970122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434063
Samples
Known GenesLRRC69
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914380
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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