A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098805



Internal ID21429780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30359305..30359356hg38UCSC Ensembl
chr17:28686323..28686374hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601726
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098805
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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