A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938238



Internal ID21358307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36429253..36429253hg38UCSC Ensembl
chr6:36397030..36397030hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202379
SamplesHG002
Known GenesPXT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938238
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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