A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938505



Internal ID21358574
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195175
SamplesHG002
Known GenesWARS
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938505
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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