A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250898



Internal ID20817938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35024886..35025470hg38UCSC Ensembl
chr1:35490487..35491071hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554047
Supporting Variants
Samples
Known GenesZMYM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250898
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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