A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747136



Internal ID20523153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136551185..136551248hg38UCSC Ensembl
chr3:136270027..136270090hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284375
Samples
Known GenesSTAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747136
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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