A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616384



Internal ID20989455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39607201..39615700hg38UCSC Ensembl
chr7:39646800..39655299hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218905
Samples
Known GenesYAE1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616384
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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