A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144657



Internal ID21420947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13925069..13925069hg38UCSC Ensembl
chr6:13925300..13925300hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626461
Supporting Variants
SamplesHG00731
Known GenesRNF182
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144657
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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