A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4810n54



Internal ID22772705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:380011..445662hg38UCSC Ensembl
chr16:430011..495662hg19UCSC Ensembl
chr16:370012..435663hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3865652
hg1965652
hg1865652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570958, nsv570957
Samples1780862415_A
Known GenesDECR2, LOC100134368, NME4, RAB11FIP3, TMEM8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4810n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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