A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3427n54



Internal ID22771322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113074031..113109612hg38UCSC Ensembl
chr13:113728345..113763926hg19UCSC Ensembl
chr13:112776346..112811927hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3835582
hg1935582
hg1835582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563267, nsv563266
Samples
Known GenesF7, MCF2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3427n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer