A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12101n54



Internal ID22779996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39379321..39386523hg38UCSC Ensembl
chr8:39236840..39244042hg19UCSC Ensembl
chr8:39355997..39363199hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg387203
hg197203
hg187203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610996, nsv610989, nsv610995, nsv611017, nsv610999, nsv610991, nsv611000, nsv610990
Samples
Known GenesADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12101n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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