A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593436



Internal ID20966507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29984608..29986687hg38UCSC Ensembl
chr17:28311626..28313705hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382080
hg192080
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241740
Samples
Known GenesEFCAB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593436
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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