A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719706



Internal ID15666976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102876836..102906096hg38UCSC Ensembl
Innerchr1:103342392..103371652hg19UCSC Ensembl
Innerchr1:103114980..103144240hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3829261
hg1929261
hg1829261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546929
Supporting Variants
Samples
Known GenesCOL11A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv719706
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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