A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449018



Internal ID21106571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28033708..28212053hg38UCSC Ensembl
chr10:28322637..28500982hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38178346
hg19178346
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179972
Samples
Known GenesMPP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449018
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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