A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151405



Internal ID20718445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155515103..155517444hg38UCSC Ensembl
chr7:155307798..155310139hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg382342
hg192342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426918
Supporting Variants
Samples
Known GenesCNPY1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151405
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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