A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15194872



Internal ID21333774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76231974..76231974hg38UCSC Ensembl
chr14:76698317..76698317hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3929934
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15194872
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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