A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582603



Internal ID20955674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19995625..19999065hg38UCSC Ensembl
chr17:19898938..19902378hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg383441
hg193441
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241490
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582603
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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