A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420176



Internal ID21077729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5295464..5329621hg38UCSC Ensembl
chr9:5295464..5329621hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3834158
hg1934158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183807
Samples
Known GenesRLN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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