A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439525



Internal ID21097078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107810065..107811509hg38UCSC Ensembl
chr9:110572346..110573790hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381445
hg191445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439525
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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