A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584201



Internal ID20957272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58545249..58546126hg38UCSC Ensembl
chr17:56622610..56623487hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38878
hg19878
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243028
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584201
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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