A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939136



Internal ID21359205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15726132..15726132hg38UCSC Ensembl
chr6:15726363..15726363hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201125
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939136
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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