A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609758



Internal ID20982829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12913496..12939147hg38UCSC Ensembl
chr7:12953121..12978772hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3825652
hg1925652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229782
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609758
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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