A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444550



Internal ID21102103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112952556..113025206hg38UCSC Ensembl
chr9:115714836..115787486hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3872651
hg1972651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175293
Samples
Known GenesZNF883
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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