A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613476



Internal ID20986547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101733182..101740484hg38UCSC Ensembl
chr7:101376462..101383764hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg387303
hg197303
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228828
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613476
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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