A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031153



Internal ID21940496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31872451..31872591hg38UCSC Ensembl
chr17:30199470..30199610hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633997
Samples
Known GenesUTP6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031153
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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