A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445823



Internal ID21103376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15833501..15835300hg38UCSC Ensembl
chr10:15875500..15877299hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978802
Samples
Known GenesFAM188A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445823
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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