A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585926



Internal ID20958997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61632472..61638728hg38UCSC Ensembl
chr17:59709833..59716089hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg386257
hg196257
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3213n223
Supporting Variantsnssv18243148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585926
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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