A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405195



Internal ID21062748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24473000..24482574hg38UCSC Ensembl
chr6:24473228..24482802hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg389575
hg199575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140660
Samples
Known GenesGPLD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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