A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444504



Internal ID21102057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6824483..6833139hg38UCSC Ensembl
chr10:6866445..6875101hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg388657
hg198657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983000
Samples
Known GenesLINC00707
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444504
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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