A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581049



Internal ID20954120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80274842..80281700hg38UCSC Ensembl
chr17:78248641..78255499hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg386859
hg196859
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3254n223
Supporting Variantsnssv18243272
Samples
Known GenesRNF213
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581049
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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