A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273769



Internal ID20840809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155114924..155115058hg38UCSC Ensembl
chr7:154906634..154906768hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560822
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273769
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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