A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489265



Internal ID22547184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201649003..201657871hg38UCSC Ensembl
chr2:202513726..202522594hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg388869
hg198869
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832367
Supporting Variants
Samples
Known GenesMPP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489265
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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