A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126125



Internal ID21469518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43087714..43087810hg38UCSC Ensembl
chr5:43087816..43087912hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574835
Supporting Variants
SamplesHG03125
Known GenesLOC100506639
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126125
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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