A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321842



Internal ID20854950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35638726..35639028hg38UCSC Ensembl
chr1:36104327..36104629hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061067
Samples
Known GenesPSMB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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