A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417615



Internal ID22475485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:136618825..136703438hg38UCSC Ensembl
chr4:137539980..137624593hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3884614
hg1984614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907226
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417615
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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