A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452163



Internal ID21109716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21715175..21716927hg38UCSC Ensembl
chr10:22004104..22005856hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381753
hg191753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979629
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452163
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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