A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573679



Internal ID20946750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71488880..71490231hg38UCSC Ensembl
chr7:70953865..70955216hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381352
hg191352
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275721
Samples
Known GenesWBSCR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573679
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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