A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437228



Internal ID21094781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101841534..101849859hg38UCSC Ensembl
chr10:103601291..103609616hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg388326
hg198326
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177351
Samples
Known GenesC10orf76, KCNIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437228
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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