A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934782



Internal ID22710114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39160203..39173015hg38UCSC Ensembl
chr17:37316456..37329268hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3812813
hg1912813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384595
Samples
Known GenesARL5C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934782
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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