A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250848



Internal ID20817888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32543791..32544580hg38UCSC Ensembl
chr1:33009392..33010181hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552755
Supporting Variants
Samples
Known GenesZBTB8A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250848
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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