A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv724899



Internal ID16018855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:154501809..154502501hg38UCSC Ensembl
Innerchr1:154474285..154474977hg19UCSC Ensembl
Innerchr1:152740909..152741601hg18UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38693
hg19693
hg18693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547954
Supporting Variants
Samples
Known GenesSHE, TDRD10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv724899
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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