A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335065



Internal ID20868256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107792426..107844602hg38UCSC Ensembl
chr1:108335048..108387224hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3852177
hg1952177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199209
Samples
Known GenesVAV3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335065
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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