A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437987



Internal ID21095540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91799601..91801300hg38UCSC Ensembl
chr10:93559358..93561057hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985372
Samples
Known GenesTNKS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437987
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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