A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577396



Internal ID20950467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30486340..30488296hg38UCSC Ensembl
chr17:28813358..28815314hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381957
hg191957
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241766
Samples
Known GenesGOSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577396
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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