A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265697



Internal ID20832737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44897258..44898407hg38UCSC Ensembl
chr4:44899275..44900424hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg381150
hg191150
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265697
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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