A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275672



Internal ID20842712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39914843..39916024hg38UCSC Ensembl
chr7:39954442..39955623hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381182
hg191182
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567416
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275672
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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