A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636808



Internal ID21585113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34876463..34876463hg38UCSC Ensembl
chr5:34876568..34876568hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138047
SamplesHG03486
Known GenesTTC23L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636808
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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