A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445626



Internal ID21103179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80334530..80337300hg38UCSC Ensembl
chr10:82094286..82097056hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg382771
hg192771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983623
Samples
Known GenesDYDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445626
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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