A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587231



Internal ID20960302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62642695..62643030hg38UCSC Ensembl
chr17:60720056..60720391hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242594
Samples
Known GenesMRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587231
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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