A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574486



Internal ID20947557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17161203..17162050hg38UCSC Ensembl
chr5:17161312..17162159hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38848
hg19848
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267632
Samples
Known GenesLOC285696
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574486
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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