A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243979



Internal ID20811019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2789376..2789907hg38UCSC Ensembl
chr18:2789374..2789905hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593541
Supporting Variants
Samples
Known GenesSMCHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243979
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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