A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439230



Internal ID21096783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69349476..69355128hg38UCSC Ensembl
chr10:71109232..71114884hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg385653
hg195653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983066
Samples
Known GenesHK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439230
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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