A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446052



Internal ID21103605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119942581..119950397hg38UCSC Ensembl
chr10:121702093..121709909hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg387817
hg197817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980461
Samples
Known GenesSEC23IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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