A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917307



Internal ID22692526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98605963..98610034hg38UCSC Ensembl
chr9:101368245..101372316hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg384072
hg194072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431026
Samples
Known GenesGABBR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917307
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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