A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274488



Internal ID20841528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141668434..141669401hg38UCSC Ensembl
chr7:141368234..141369201hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38968
hg19968
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565777
Supporting Variants
Samples
Known GenesKIAA1147
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274488
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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