A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572596



Internal ID20945667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56258115..56258997hg38UCSC Ensembl
chr5:55553942..55554824hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38883
hg19883
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5763n223
Supporting Variantsnssv18269116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572596
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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