A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944652



Internal ID22720120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71071737..71072786hg38UCSC Ensembl
chr17:69067878..69068927hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388742
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944652
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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