A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441428



Internal ID21098981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13906501..14013525hg38UCSC Ensembl
chr10:13948501..14055524hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38107025
hg19107024
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196430
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441428
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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