A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608975



Internal ID20982046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:128311348..128312003hg38UCSC Ensembl
chr6:128632493..128633148hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137731
Samples
Known GenesPTPRK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608975
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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