A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433694



Internal ID21091247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129197689..129201949hg38UCSC Ensembl
chr7:128837530..128841790hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg384261
hg194261
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231410
Samples
Known GenesSMO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433694
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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