A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222402



Internal ID20789442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:54170455..58863076hg38UCSC Ensembl
chr10:55930215..60622836hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg384692622
hg194692622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584881
Supporting Variants
Samples
Known GenesBICC1, CISD1, FAM133CP, IPMK, MIR3924, MTRNR2L5, PCDH15, TFAM, UBE2D1, ZWINT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222402
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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