A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159555



Internal ID20726595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74631693..74634233hg38UCSC Ensembl
chr7:74046009..74048549hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg382541
hg192541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159555
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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