A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426131



Internal ID21083684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2836213..2836705hg38UCSC Ensembl
chr9:2836213..2836705hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182342
Samples
Known GenesKIAA0020
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426131
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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