A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938957



Internal ID21359026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45884971..45884971hg38UCSC Ensembl
chr6:45852708..45852708hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202773
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938957
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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