A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154095



Internal ID21425101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121648772..121649502hg38UCSC Ensembl
chr7:121288826..121289556hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569592
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154095
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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