A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616259



Internal ID20989330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3034451..3050025hg38UCSC Ensembl
chr7:3074085..3089659hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3815575
hg1915575
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225464
Samples
Known GenesCARD11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616259
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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