A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747954



Internal ID20523977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24964830..24965508hg38UCSC Ensembl
chr4:24966452..24967130hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266427
Samples
Known GenesCCDC149
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747954
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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