A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445193



Internal ID21102746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71356744..71374184hg38UCSC Ensembl
chr10:73116501..73133941hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3817441
hg1917441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983557
Samples
Known GenesSLC29A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445193
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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