A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143281



Internal ID21453807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69425805..69426351hg38UCSC Ensembl
chr7:68890791..68891337hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580034
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143281
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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