A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443819



Internal ID21101372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21706482..21710462hg38UCSC Ensembl
chr10:21995411..21999391hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg383981
hg193981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979628
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443819
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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