A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178472



Internal ID20745512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67514701..67556800hg38UCSC Ensembl
chr15:67807039..67849138hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3842100
hg1942100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507812
Supporting Variants
Samples
Known GenesC15orf61, IQCH-AS1, MAP2K5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178472
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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