A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144875



Internal ID21465386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155363067..155363067hg38UCSC Ensembl
chr7:155155762..155155762hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631488
Supporting Variants
SamplesHG03065
Known GenesBLACE
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144875
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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