A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565595



Internal ID20938666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15599679..15599783hg38UCSC Ensembl
chr7:15639304..15639408hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565595
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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