A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501853



Internal ID20875091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18905140..18906332hg38UCSC Ensembl
chr17:18808453..18809645hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381193
hg191193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034770
Samples
Known GenesPRPSAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501853
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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