A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589212



Internal ID20962283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76849623..76850969hg38UCSC Ensembl
chr17:74845705..74847051hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg381347
hg191347
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243220
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589212
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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