A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561629



Internal ID20934700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92600900..92601377hg38UCSC Ensembl
chr7:92230214..92230691hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561629
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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