A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186229



Internal ID20753270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79273001..79324700hg38UCSC Ensembl
chr15:79565343..79617042hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3851700
hg1951700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499898
Supporting Variants
Samples
Known GenesANKRD34C, LOC729911, TMED3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186229
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00048


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