A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532443



Internal ID21856799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237521759..237521820hg38UCSC Ensembl
chr2:238430402..238430463hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5988119
Supporting Variants
Samples
Known GenesMLPH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532443
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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