A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149972



Internal ID20717012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:11521462..11521709hg38UCSC Ensembl
chr7:11561089..11561336hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603506
Supporting Variants
Samples
Known GenesTHSD7A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.17232


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