A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591726



Internal ID20964797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75365303..75381788hg38UCSC Ensembl
chr17:73361384..73377869hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3816486
hg1916486
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244612
Samples
Known GenesGRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591726
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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