A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501682



Internal ID22559621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160490799..160499229hg38UCSC Ensembl
chr6:160911831..160920261hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg388431
hg198431
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844689
Supporting Variants
Samples
Known GenesLPAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501682
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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