A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129256



Internal ID21468092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162739933..162741007hg38UCSC Ensembl
chr5:162166939..162168013hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381075
hg191075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579009
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129256
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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