A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605960



Internal ID21554265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195209961..195209961hg38UCSC Ensembl
chr3:194930690..194930690hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129090
SamplesNA19239
Known GenesXXYLT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605960
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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