A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038834



Internal ID21948177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39795801..39795897hg38UCSC Ensembl
chr17:37952054..37952150hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630428
Samples
Known GenesIKZF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038834
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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