A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439126



Internal ID21096679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73572538..73573050hg38UCSC Ensembl
chr9:76187454..76187966hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439126
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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