A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735986



Internal ID20511929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239068830..239068927hg38UCSC Ensembl
chr2:239990526..239990623hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295814
Samples
Known GenesHDAC4, MIR4440
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735986
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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