A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442960



Internal ID21100513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100242691..100243405hg38UCSC Ensembl
chr10:102002448..102003162hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977125
Samples
Known GenesCWF19L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442960
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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