A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430106



Internal ID21087659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15005245..15006496hg38UCSC Ensembl
chr9:15005243..15006494hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg381252
hg191252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175016
Samples
Known GenesLOC389705
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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