A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095142



Internal ID21450799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40848845..40848845hg38UCSC Ensembl
chr17:39005097..39005097hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659572
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095142
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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