A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844367



Internal ID22619302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:128499059..128501358hg38UCSC Ensembl
chr6:128820204..128822503hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501170, nssv17501169
Samples
Known GenesPTPRK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844367
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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