A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv168n54



Internal ID20133592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16898769..16932783hg38UCSC Ensembl
chr1:17225264..17259278hg19UCSC Ensembl
chr1:17097851..17131865hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3834015
hg1934015
hg1834015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545679, nsv545676
Samples
Known GenesCROCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv168n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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