A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441622



Internal ID21099175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96307630..96314619hg38UCSC Ensembl
chr10:98067387..98074376hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg386990
hg196990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985918
Samples
Known GenesDNTT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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