A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272369



Internal ID20839409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123937578..123939139hg38UCSC Ensembl
chr7:123577632..123579193hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg381562
hg191562
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567115
Supporting Variants
Samples
Known GenesSPAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272369
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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