A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451819



Internal ID21109372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73597801..73749000hg38UCSC Ensembl
chr10:75357559..75508758hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38151200
hg19151200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv810n223
Supporting Variantsnssv18186519
Samples
Known GenesAGAP5, BMS1P4, GLUD1P3, MYOZ1, SEC24C, SYNPO2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451819
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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