A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940596



Internal ID22716007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37807658..37809618hg38UCSC Ensembl
chr17:36167627..36169335hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381961
hg191709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378978
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940596
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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