A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034493



Internal ID21943836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37807683..37809630hg38UCSC Ensembl
chr17:36167652..36169335hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381948
hg191684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034493
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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