A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510005



Internal ID20883318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102154801..102164300hg38UCSC Ensembl
chr14:102621138..102630637hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg389500
hg199500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2245n223
Supporting Variantsnssv18015629
Samples
Known GenesWDR20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510005
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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