A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452968



Internal ID21110521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130771815..130783727hg38UCSC Ensembl
chr9:133647202..133659114hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg3811913
hg1911913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176934
Samples
Known GenesABL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452968
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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