A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445879



Internal ID21103432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133892274..133904326hg38UCSC Ensembl
chr9:136757396..136769448hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3812053
hg1912053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175224
Samples
Known GenesVAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445879
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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