A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141293



Internal ID21454576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30526022..30526145hg38UCSC Ensembl
chr7:30565638..30565761hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584445
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141293
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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