A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287544



Internal ID20496762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173932361..173936192hg38UCSC Ensembl
chr2:174797089..174800920hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg383832
hg193832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739182
Supporting Variants
Samples
Known GenesSP3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287544
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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