A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586314



Internal ID20959385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50760052..50761312hg38UCSC Ensembl
chr17:48837413..48838673hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg381261
hg191261
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3184n223
Supporting Variantsnssv18245173
Samples
Known GenesLINC00483
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586314
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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