A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151913



Internal ID21424138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42734099..42734099hg38UCSC Ensembl
chr7:42773698..42773698hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640585
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151913
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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