A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721297



Internal ID144963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10276000..10294000hg38UCSC Ensembl
chr19:10386676..10404676hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3818001
hg1918001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144509
Supporting Variants
Samples
Known GenesICAM1, ICAM4, ICAM5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721297
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004558


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