A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572656



Internal ID20945727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:71504079..71505142hg38UCSC Ensembl
chr5:70799906..70800969hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg381064
hg191064
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267028
Samples
Known GenesBDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572656
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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