A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156090



Internal ID21463710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77523803..77523803hg38UCSC Ensembl
chr7:77153120..77153120hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625225
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156090
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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