A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4825n54



Internal ID20138249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:661905..761746hg38UCSC Ensembl
chr16:711905..811746hg19UCSC Ensembl
chr16:651906..751747hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3899842
hg1999842
hg1899842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571017, nsv571020
Samples1780862416_A
Known GenesCCDC78, FAM173A, FBXL16, HAGHL, JMJD8, METRN, MSLN, NARFL, RHBDL1, RHOT2, STUB1, WDR24, WDR90
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4825n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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