A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152379



Internal ID20719419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135706205..135710391hg38UCSC Ensembl
chr7:135390953..135395139hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg384187
hg194187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428828
Supporting Variants
Samples
Known GenesSLC13A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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