A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374826



Internal ID22600495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:47760609..47808195hg38UCSC Ensembl
chr14:48229812..48277398hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3847587
hg1947587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938242
Supporting Variants
Samples
Known GenesLINC00648, MIR548Y
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374826
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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