A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572058



Internal ID20945129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155018970..155020072hg38UCSC Ensembl
chr7:154810680..154811782hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg381103
hg191103
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572058
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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