A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593999



Internal ID20967070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37048372..37049326hg38UCSC Ensembl
chr17:35405670..35406624hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38955
hg19955
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242208
Samples
Known GenesAATF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593999
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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