A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037556



Internal ID21946899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:44966257..44969312hg38UCSC Ensembl
chr14:45435460..45438515hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg383056
hg193056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598430
Samples
Known GenesFAM179B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037556
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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