A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442817



Internal ID21100370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103102701..103103600hg38UCSC Ensembl
chr10:104862458..104863357hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977722
Samples
Known GenesNT5C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442817
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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