A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953154



Internal ID21373224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11491591..11491591hg38UCSC Ensembl
chr6:11491824..11491824hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38719
hg19719
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201899
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953154
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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