A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555712



Internal ID20928783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62092425..62334777hg38UCSC Ensembl
chr4:62958143..63200495hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38242353
hg19242353
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265883
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555712
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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