A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609050



Internal ID20982121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:118124400..118188092hg38UCSC Ensembl
chr7:117764454..117828146hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3863693
hg1963693
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222673
Samples
Known GenesNAA38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609050
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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