A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439474



Internal ID21097027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134897301..134905800hg38UCSC Ensembl
chr9:137789147..137797646hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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