A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603218



Internal ID21795265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51832694..51838899hg38UCSC Ensembl
chr14:52299412..52305617hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg386206
hg196206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033855
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603218
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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