A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577055



Internal ID20950126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61601807..61602353hg38UCSC Ensembl
chr17:59679168..59679714hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577055
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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