A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031979



Internal ID21941322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5431224..5431358hg38UCSC Ensembl
chr17:5334544..5334678hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636720
Samples
Known GenesRPAIN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031979
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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