A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909570



Internal ID22684780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39242601..39245214hg38UCSC Ensembl
chr8:39100120..39102733hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg382614
hg192614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435876
Samples
Known GenesADAM32
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909570
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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