A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666804



Internal ID21615112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103911636..103911960hg38UCSC Ensembl
chr7:14882950..14883258hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38325
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165183
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666804
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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