A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007060



Internal ID21916403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160106962..160111278hg38UCSC Ensembl
chr5:159533969..159538285hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg384317
hg194317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558028
Samples
Known GenesPWWP2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007060
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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