A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235184



Internal ID20802224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81688862..81961146hg38UCSC Ensembl
chr8:82601097..82873381hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38272285
hg19272285
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431510
Supporting Variants
Samples
Known GenesCHMP4C, SLC10A5, SNX16, ZFAND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235184
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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