A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589691



Internal ID20962762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30097957..30098360hg38UCSC Ensembl
chr17:28424975..28425378hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3071n223
Supporting Variantsnssv18241744
Samples
Known GenesEFCAB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589691
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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