A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485535



Internal ID22543446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43911526..43945867hg38UCSC Ensembl
chr2:44138665..44173006hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3834342
hg1934342
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5833349
Supporting Variants
Samples
Known GenesLRPPRC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485535
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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