A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006178



Internal ID21915521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147734527..147734640hg38UCSC Ensembl
chr5:147114090..147114203hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564728
Samples
Known GenesJAKMIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006178
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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