A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100883



Internal ID21508931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3600749..3600749hg38UCSC Ensembl
chr18:3600747..3600747hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659471
Supporting Variants
SamplesNA20847
Known GenesDLGAP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100883
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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