A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585960



Internal ID20959031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53104188..53547682hg38UCSC Ensembl
chr17:51181549..51625043hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38443495
hg19443495
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585960
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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