A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444035



Internal ID21101588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132792490..132989489hg38UCSC Ensembl
chr10:134605994..134802993hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38197000
hg19197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv920n223
Supporting Variantsnssv18194694
Samples
Known GenesLOC399829, TTC40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444035
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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