A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544925



Internal ID15985648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:934170..943937hg38UCSC Ensembl
Innerchr1:869550..879317hg19UCSC Ensembl
Innerchr1:859413..869180hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg389768
hg199768
hg189768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv15n54
Supporting Variantsnssv708383, nssv708378, nssv708386, nssv708379, nssv708374, nssv708376, nssv708385, nssv708380, nssv708377, nssv708382, nssv708384, nssv708381, nssv708375
Samples
Known GenesSAMD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544925
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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