A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922137



Internal ID22697362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37848197..37852054hg38UCSC Ensembl
chr8:37705715..37709572hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg383858
hg193858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431090
Samples
Known GenesBRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922137
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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