A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv171n54



Internal ID20133595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16919140..16936882hg38UCSC Ensembl
chr1:17245635..17263377hg19UCSC Ensembl
chr1:17118222..17135964hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3817743
hg1917743
hg1817743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545689, nsv545687, nsv545688, nsv545686
Samples
Known GenesCROCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv171n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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