A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565064



Internal ID20938135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83113759..83115262hg38UCSC Ensembl
chr5:82409578..82411081hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg381504
hg191504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269633
Samples
Known GenesXRCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565064
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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