A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920312



Internal ID22695535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39135501..39245019hg38UCSC Ensembl
chr8:38993020..39102538hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38109519
hg19109519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430243
Samples
Known GenesADAM32
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920312
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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