A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100807



Internal ID21455294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2614527..2614607hg38UCSC Ensembl
chr18:2614526..2614606hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599998
Supporting Variants
SamplesHG02011
Known GenesNDC80
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100807
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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