A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276029



Internal ID20843069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45520461..45521027hg38UCSC Ensembl
chr7:45560060..45560626hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565129
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276029
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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