A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445919



Internal ID21103472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34628103..34923856hg38UCSC Ensembl
chr10:34917031..35212784hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38295754
hg19295754
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv680n223
Supporting Variantsnssv18192245
Samples
Known GenesPARD3, PARD3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445919
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer