A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544898



Internal ID15985621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:924665..943937hg38UCSC Ensembl
Innerchr1:860045..879317hg19UCSC Ensembl
Innerchr1:849908..869180hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3819273
hg1919273
hg1819273
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv707679
Samples
Known GenesSAMD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544898
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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