A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141197



Internal ID21448017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36435382..36435382hg38UCSC Ensembl
chr7:36474991..36474991hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5629944
Supporting Variants
SamplesHG00733
Known GenesANLN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141197
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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