A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094356



Internal ID21470337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76124324..76124324hg38UCSC Ensembl
chr17:74120405..74120405hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654389
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094356
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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