A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555996



Internal ID20929067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:71496038..71496734hg38UCSC Ensembl
chr5:70791865..70792561hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267026
Samples
Known GenesBDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555996
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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