A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938533



Internal ID21358603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87869372..87869372hg38UCSC Ensembl
chr6:88579090..88579090hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202026
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938533
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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