A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613395



Internal ID20986466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21961723..21998498hg38UCSC Ensembl
chr7:22001341..22038116hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3836776
hg1936776
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227169
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613395
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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