A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903814



Internal ID22678985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36398021..36398303hg38UCSC Ensembl
chr6:36365798..36366080hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445355
Samples
Known GenesPXT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903814
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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