A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439347



Internal ID21096900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116437550..116438947hg38UCSC Ensembl
chr10:118197062..118198459hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381398
hg191398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978257
Samples
Known GenesPNLIPRP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439347
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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