A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286132



Internal ID20495350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:212763550..212763644hg38UCSC Ensembl
chr2:213628274..213628368hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738380
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286132
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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