A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372915



Internal ID21030468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127101270..127152800hg38UCSC Ensembl
chr3:126820113..126871643hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3851531
hg1951531
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372915
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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