A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577297



Internal ID20950368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8661353..8662272hg38UCSC Ensembl
chr17:8564671..8565590hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38920
hg19920
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577297
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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