A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573793



Internal ID20946864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73610969..73611541hg38UCSC Ensembl
chr6:74320692..74321264hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272049
Samples
Known GenesSLC17A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573793
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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