A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619344



Internal ID20992415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123565606..123568238hg38UCSC Ensembl
chr7:123205660..123208292hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg382633
hg192633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619344
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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