A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591993



Internal ID20965064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31940741..31941415hg38UCSC Ensembl
chr17:30267760..30268434hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244406
Samples
Known GenesSUZ12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591993
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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