A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438341



Internal ID21095894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69097343..69097733hg38UCSC Ensembl
chr10:70857099..70857489hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983061
Samples
Known GenesSRGN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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