A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229607



Internal ID20796647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110858982..111100981hg38UCSC Ensembl
chr13:111511329..111753328hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38242000
hg19242000
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584186
Supporting Variants
Samples
Known GenesANKRD10, LINC00346
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229607
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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