A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617923



Internal ID20990994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13718774..13935431hg38UCSC Ensembl
chr7:13758399..13975056hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38216658
hg19216658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227732
Samples
Known GenesETV1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617923
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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