A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451557



Internal ID21109110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88192801..88214200hg38UCSC Ensembl
chr10:89952558..89973957hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3821400
hg1921400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv845n223
Supporting Variantsnssv17984852
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451557
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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