A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107779



Internal ID22017012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34743532..36146243hg38UCSC Ensembl
chr18:32323496..33726206hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381402712
hg191402711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630940
Samples
Known GenesC18orf21, DTNA, ELP2, GALNT1, INO80C, MAPRE2, MIR187, MIR3975, RPRD1A, SLC39A6, ZNF24, ZNF271, ZNF396, ZNF397, ZSCAN30
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107779
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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