A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450041



Internal ID21107594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81100190..81109798hg38UCSC Ensembl
chr9:83715105..83724713hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg389609
hg199609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184528
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450041
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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