A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218142



Internal ID20785182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79542962..80217143hg38UCSC Ensembl
chr10:81302718..81976899hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38674182
hg19674182
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595201
Supporting Variants
Samples
Known GenesANXA11, BEND3P3, LINC00857, LOC100288974, LOC642361, MBL1P, NUTM2B, PLAC9, SFTPA1, SFTPA2, SFTPD, TMEM254, TMEM254-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218142
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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