A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153998



Internal ID20721038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148997012..149003201hg38UCSC Ensembl
chr7:148694104..148700293hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386190
hg196190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434277
Supporting Variants
Samples
Known GenesPDIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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