A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586126



Internal ID20959197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31785259..32556165hg38UCSC Ensembl
chr18:29365222..30136128hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38770907
hg19770907
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244038
Samples
Known GenesGAREM, MEP1B, RNF125, RNF138, TRAPPC8, WBP11P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586126
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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