A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029848



Internal ID21939191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44160333..44160959hg38UCSC Ensembl
chr17:42237701..42238327hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632900
Samples
Known GenesC17orf53
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029848
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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