A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327622



Internal ID20860762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:88720901..88735300hg38UCSC Ensembl
chr1:89186584..89200983hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3814400
hg1914400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064876
Samples
Known GenesPKN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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