A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544907



Internal ID16332316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:929558..943937hg38UCSC Ensembl
Innerchr1:864938..879317hg19UCSC Ensembl
Innerchr1:854801..869180hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3814380
hg1914380
hg1814380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8n54
Supporting Variantsnssv707702
Samples
Known GenesSAMD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544907
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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