A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601981



Internal ID20975052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161412194..161571199hg38UCSC Ensembl
chr6:161833226..161992231hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38159006
hg19159006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139205
Samples
Known GenesPARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601981
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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