A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570342



Internal ID20943413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111827690..111828189hg38UCSC Ensembl
chr5:111163387..111163886hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267175
Samples
Known GenesNREP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570342
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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