A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615691



Internal ID20988762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162020559..162646992hg38UCSC Ensembl
chr6:162441591..163068024hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38626434
hg19626434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139241
Samples
Known GenesPARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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