A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406403



Internal ID22464273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27512067..27512362hg38UCSC Ensembl
chr2:27734934..27735229hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874890
Supporting Variants
Samples
Known GenesGCKR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406403
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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