A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906155



Internal ID22681351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160655486..160667303hg38UCSC Ensembl
chr5:160082493..160094310hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3811818
hg1911818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416533
Samples
Known GenesATP10B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906155
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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