A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979626



Internal ID20546666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21560701..21566800hg38UCSC Ensembl
chr10:21849630..21855729hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445979
Supporting Variants
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979626
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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