A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583661



Internal ID20956732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5060595..5061389hg38UCSC Ensembl
chr17:4963890..4964684hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245162
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583661
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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