A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577352



Internal ID20950423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10897695..10928795hg38UCSC Ensembl
chr17:10801012..10832112hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3831101
hg1931101
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577352
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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