A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490534



Internal ID267787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38498789..38685381hg38UCSC Ensembl
chr9:38498786..38685378hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38186593
hg19186593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022900
Samples
Known GenesANKRD18A, FAM201A, FAM95C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490534
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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