A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089385



Internal ID21491576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4138890..4139131hg38UCSC Ensembl
chr17:4042184..4042425hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594712
Supporting Variants
SamplesNA19238
Known GenesZZEF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089385
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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