A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273605



Internal ID20840645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107937632..107942595hg38UCSC Ensembl
chr7:107578077..107583040hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg384964
hg194964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573813
Supporting Variants
Samples
Known GenesLAMB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273605
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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