A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439988



Internal ID21097541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103827651..103870756hg38UCSC Ensembl
chr10:105587409..105630514hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3843106
hg1943106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193706
Samples
Known GenesSH3PXD2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439988
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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