A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582656



Internal ID20955727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39004848..39005896hg38UCSC Ensembl
chr17:37161101..37162149hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3103n223
Supporting Variantsnssv18242251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582656
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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