A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152487



Internal ID20719527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143444149..143444459hg38UCSC Ensembl
chr7:143141242..143141552hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424233
Supporting Variants
Samples
Known GenesEPHA1-AS1, TAS2R60
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152487
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00129


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