A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv169n54



Internal ID20133593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16912199..16930807hg38UCSC Ensembl
chr1:17238694..17257302hg19UCSC Ensembl
chr1:17111281..17129889hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3818609
hg1918609
hg1818609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545680, nsv545683
Samples
Known GenesCROCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv169n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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