A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615705



Internal ID20988776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94027609..94040006hg38UCSC Ensembl
chr7:93656921..93669318hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3812398
hg1912398
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225609
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615705
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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