A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036671



Internal ID21946014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14615702..14616551hg38UCSC Ensembl
chr17:14519019..14519868hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38850
hg19850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036671
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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