A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449828



Internal ID21107381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102034537..102092905hg38UCSC Ensembl
chr10:103794294..103852662hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3858369
hg1958369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194135
Samples
Known GenesC10orf76, HPS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449828
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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