A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001442



Internal ID21910785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112913528..112914131hg38UCSC Ensembl
chr5:112249225..112249828hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545225
Samples
Known GenesREEP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001442
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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