A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173025



Internal ID15873692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:76482359..76510837hg38UCSC Ensembl
Innerchr1:76948044..76976522hg19UCSC Ensembl
Innerchr1:76720632..76749110hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3828479
hg1928479
hg1828479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546587
Supporting Variants
SamplesHGDP00307
Known GenesST6GALNAC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173025
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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