A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842072



Internal ID22617007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156958405..156967131hg38UCSC Ensembl
chr5:156385416..156394142hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg388727
hg198727
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496382
Samples
Known GenesTIMD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842072
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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