A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603649



Internal ID20976720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:33445435..33620455hg38UCSC Ensembl
chr7:33485047..33660067hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38175021
hg19175021
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228855
Samples
Known GenesBBS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603649
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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