A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574031



Internal ID20947102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:159457348..159458416hg38UCSC Ensembl
chr4:160378500..160379568hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381069
hg191069
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5528n223
Supporting Variantsnssv18264257
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574031
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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