A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620357



Internal ID21568662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195087451..195087451hg38UCSC Ensembl
chr3:194808180..194808180hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129371
SamplesHG02011
Known GenesXXYLT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620357
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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