A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4907n54



Internal ID18997083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10388455..10504610hg38UCSC Ensembl
chr16:10482312..10598467hg19UCSC Ensembl
chr16:10389813..10505968hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38116156
hg19116156
hg18116156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571449, nsv571450
Samples
Known GenesATF7IP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4907n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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