A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557628



Internal ID20930699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56936016..56936691hg38UCSC Ensembl
chr4:57802182..57802857hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38676
hg19676
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265815
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557628
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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