A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14241836



Internal ID21309094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:36104694..36112411hg38UCSC Ensembl
Outerchr2:36097392..36123960hg38UCSC Ensembl
Innerchr2:36331837..36339554hg19UCSC Ensembl
Outerchr2:36324535..36351103hg19UCSC Ensembl
Innerchr2:36185341..36193058hg18UCSC Ensembl
Outerchr2:36178039..36204607hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3826569
hg1926569
hg1826569
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170091
Supporting Variants
SamplesNGO_47
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14241836
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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