A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155727



Internal ID20722767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145697301..145697900hg38UCSC Ensembl
chr7:145394394..145394993hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426525
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155727
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.06245


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