A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9n54



Internal ID20133433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:925754..952840hg38UCSC Ensembl
chr1:861134..888220hg19UCSC Ensembl
chr1:850997..878083hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3827087
hg1927087
hg1827087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv544902, nsv544903
Samples
Known GenesNOC2L, SAMD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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