A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087791



Internal ID21475316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15979643..15979770hg38UCSC Ensembl
chr17:15882957..15883084hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589891
Supporting Variants
SamplesHG03371
Known GenesZSWIM7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087791
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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