A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612906



Internal ID20985977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51157001..51161100hg38UCSC Ensembl
chr7:51224698..51228797hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223857
Samples
Known GenesCOBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612906
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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