A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271791



Internal ID20838831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132865446..132876610hg38UCSC Ensembl
chr7:132550206..132561370hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3811165
hg1911165
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559493
Supporting Variants
Samples
Known GenesCHCHD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271791
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00013


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