A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576839



Internal ID20949910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39004944..39006096hg38UCSC Ensembl
chr17:37161197..37162349hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381153
hg191153
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3103n223
Supporting Variantsnssv18242252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576839
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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