A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444927



Internal ID21102480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69264305..69277912hg38UCSC Ensembl
chr10:71024061..71037668hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3813608
hg1913608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195295
Samples
Known GenesHK1, HKDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444927
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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