A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250899



Internal ID20817939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35028327..35028586hg38UCSC Ensembl
chr1:35493928..35494187hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544047
Supporting Variants
Samples
Known GenesZMYM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250899
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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