A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101127



Internal ID21471423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33786096..33791293hg38UCSC Ensembl
chr18:31366060..31371257hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg385198
hg195198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592265
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101127
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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