A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936695



Internal ID22712053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32928768..32928939hg38UCSC Ensembl
chr17:31255786..31255957hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379647
Samples
Known GenesTMEM98
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936695
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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