A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608229



Internal ID20981300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15202682..15273241hg38UCSC Ensembl
chr7:15242307..15312866hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3870560
hg1970560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228989
Samples
Known GenesAGMO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608229
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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