A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571514



Internal ID20944585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:110303172..110312994hg38UCSC Ensembl
chr5:109638873..109648695hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg389823
hg199823
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571514
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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