A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574118



Internal ID20947189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162009971..162012683hg38UCSC Ensembl
chr5:161436977..161439689hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382713
hg192713
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6007n223
Supporting Variantsnssv18267463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574118
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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