A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922805



Internal ID22698030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37826838..37826900hg38UCSC Ensembl
chr8:37684356..37684418hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441255
Samples
Known GenesGPR124
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922805
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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