A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101864



Internal ID21485468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56689828..56689828hg38UCSC Ensembl
chr18:54357059..54357059hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662021
Supporting Variants
SamplesNA12878
Known GenesWDR7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101864
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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