A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442656



Internal ID21100209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121974001..121975600hg38UCSC Ensembl
chr10:123733516..123735115hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193952
Samples
Known GenesNSMCE4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442656
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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