A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442500



Internal ID21100053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11606201..11611200hg38UCSC Ensembl
chr10:11648200..11653199hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188635
Samples
Known GenesUSP6NL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442500
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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