A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617821



Internal ID20990892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161808905..162125646hg38UCSC Ensembl
chr6:162229937..162546678hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38316742
hg19316742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139222
Samples
Known GenesPARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617821
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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