A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435774



Internal ID21093327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31028501..31035500hg38UCSC Ensembl
chr10:31317430..31324429hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188748
Samples
Known GenesZNF438
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435774
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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