A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263737



Internal ID20830777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128013982..128015077hg38UCSC Ensembl
chr4:128935137..128936232hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg381096
hg191096
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559799
Supporting Variants
Samples
Known GenesC4orf29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263737
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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