A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435787



Internal ID21093340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:82104301..82105600hg38UCSC Ensembl
chr10:83864057..83865356hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984121
Samples
Known GenesNRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435787
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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