A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250415



Internal ID20817455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35697174..35700464hg38UCSC Ensembl
chr1:36162775..36166065hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383291
hg193291
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537391
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250415
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00051


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