A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555648



Internal ID20928232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14101290..14101731hg38UCSC Ensembl
chr5:14101399..14101840hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267516
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555648
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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