A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295690



Internal ID20504908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61447825..61452435hg38UCSC Ensembl
chr2:61674960..61679570hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg384611
hg194611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747314
Supporting Variants
Samples
Known GenesUSP34
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295690
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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