A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580754



Internal ID20953825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37028445..37029455hg38UCSC Ensembl
chr17:35385742..35386752hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381011
hg191011
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242207
Samples
Known GenesAATF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580754
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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