A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558661



Internal ID20931732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140942496..140943029hg38UCSC Ensembl
chr7:140642296..140642829hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558661
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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