A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912574



Internal ID22687790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129636326..129636547hg38UCSC Ensembl
chr9:132398605..132398826hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435810
Samples
Known GenesASB6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912574
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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