A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15195175



Internal ID21334079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100345064..100345064hg38UCSC Ensembl
chr14:100811401..100811401hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938505
Supporting Variants
SamplesHG002
Known GenesWARS
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15195175
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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