A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14246491



Internal ID21310270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109700332..109703659hg38UCSC Ensembl
Outerchr1:109700331..109707613hg38UCSC Ensembl
Innerchr1:110242954..110246281hg19UCSC Ensembl
Outerchr1:110242953..110250235hg19UCSC Ensembl
Innerchr1:110044477..110047804hg18UCSC Ensembl
Outerchr1:110044476..110051758hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg387283
hg197283
hg187283
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170282
Supporting Variants
SamplesNGO_6
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14246491
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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