A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247978



Internal ID20815018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16356642..16357245hg38UCSC Ensembl
chr1:16683137..16683740hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554004
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247978
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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