A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439441



Internal ID21096994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46136401..46271400hg38UCSC Ensembl
chr10:47529170..47642636hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38135000
hg19113467
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183616
Samples
Known GenesANTXRLP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439441
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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