A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933630



Internal ID22708944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36934361..36935461hg38UCSC Ensembl
chr17:35291661..35292761hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933630
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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