A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617047



Internal ID20990118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83176999..83195467hg38UCSC Ensembl
chr7:82806315..82824783hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3818469
hg1918469
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225314
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617047
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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