A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003765



Internal ID21913108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160423177..160423236hg38UCSC Ensembl
chr5:159850184..159850243hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570481
Samples
Known GenesPTTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003765
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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