A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903894



Internal ID22679066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:118282841..118282934hg38UCSC Ensembl
chr5:117618536..117618629hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412977
Samples
Known GenesLOC100505811
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903894
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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