A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591090



Internal ID20964161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13814902..13815530hg38UCSC Ensembl
chr17:13718219..13718847hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241344
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591090
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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