A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574517



Internal ID20947588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56869878..56874358hg38UCSC Ensembl
chr4:57736044..57740524hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg384481
hg194481
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574517
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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