A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11627n54



Internal ID22779522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142040277..142094990hg38UCSC Ensembl
chr7:141740077..141794790hg19UCSC Ensembl
chr7:141386546..141441259hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3854714
hg1954714
hg1854714
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608504, nsv608503
SamplesNINDS_22
Known GenesMGAM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11627n54
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