A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445861



Internal ID21103414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34684709..34773092hg38UCSC Ensembl
chr10:34973637..35062020hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3888384
hg1988384
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192665
Samples
Known GenesPARD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445861
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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