A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443144



Internal ID21100697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80476547..80481823hg38UCSC Ensembl
chr10:82236303..82241579hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg385277
hg195277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983624
Samples
Known GenesTSPAN14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443144
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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