A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924618



Internal ID22699845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10922575..10922651hg38UCSC Ensembl
chr8:10780085..10780161hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438560
Samples
Known GenesXKR6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924618
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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