A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084914



Internal ID21401196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68256082..68256142hg38UCSC Ensembl
chr17:66252223..66252283hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587799
Supporting Variants
SamplesHG00096
Known GenesAMZ2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084914
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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