A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452829



Internal ID22510702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97441026..97459470hg38UCSC Ensembl
chr10:99200783..99219227hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3818445
hg1918445
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851103
Supporting Variants
Samples
Known GenesEXOSC1, MMS19, ZDHHC16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452829
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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