A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242637



Internal ID21307312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:178984611..179007594hg38UCSC Ensembl
Outerchr1:178972472..179007596hg38UCSC Ensembl
Innerchr1:178953746..178976729hg19UCSC Ensembl
Outerchr1:178941607..178976731hg19UCSC Ensembl
Innerchr1:177220369..177243352hg18UCSC Ensembl
Outerchr1:177208230..177243354hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3835125
hg1935125
hg1835125
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170067
Supporting Variants
SamplesNGO_33
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14242637
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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