A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144756



Internal ID21508949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42734099..42734099hg38UCSC Ensembl
chr7:42773698..42773698hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640585
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144756
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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