A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757078



Internal ID20532938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57127201..57127201hg38UCSC Ensembl
chr3:57161229..57161229hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295711
Samples
Known GenesIL17RD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757078
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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