A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441606



Internal ID21099159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92915801..92917500hg38UCSC Ensembl
chr9:95678083..95679782hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182562
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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