A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906494



Internal ID22681695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168155444..168155531hg38UCSC Ensembl
chr4:169076595..169076682hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410190
Samples
Known GenesANXA10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906494
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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