A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2799953



Internal ID21245292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55208378..55208670hg38UCSC Ensembl
chr19:55719746..55720038hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13692919
Samples
Known GenesPTPRH
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2799953
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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