A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154308



Internal ID21413162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156053082..156053160hg38UCSC Ensembl
chr7:155845776..155845854hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567321
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154308
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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