A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155267



Internal ID20722307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139493414..139510506hg38UCSC Ensembl
chr7:139178160..139195252hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3817093
hg1917093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432161
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155267
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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