A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934708



Internal ID21354778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2504884..2504884hg38UCSC Ensembl
chr6:2505118..2505118hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201875
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934708
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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