A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10097n54



Internal ID20143521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140849850..140856743hg38UCSC Ensembl
chr5:140229435..140236328hg19UCSC Ensembl
chr5:140209619..140216512hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg386894
hg196894
hg186894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv599861, nsv599862, nsv599860, nsv599863
Samples
Known GenesPCDHA1, PCDHA10, PCDHA2, PCDHA3, PCDHA4, PCDHA5, PCDHA6, PCDHA7, PCDHA8, PCDHA9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10097n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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