A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746137



Internal ID21393068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:136112431..136138430hg38UCSC Ensembl
chr2:136870001..136896000hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3826000
hg1926000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433585
Supporting Variants
SamplesSMI041
Known GenesCXCR4
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746137
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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