A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092683



Internal ID21448687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57649228..57649444hg38UCSC Ensembl
chr17:55726589..55726805hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594790
Supporting Variants
SamplesHG00864
Known GenesMSI2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092683
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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