A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11715n54



Internal ID22779610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149749157..149816064hg38UCSC Ensembl
chr7:149446246..149513152hg19UCSC Ensembl
chr7:149077179..149144085hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3866908
hg1966907
hg1866907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608984, nsv608981
SamplesHGDP00830
Known GenesSSPO, ZNF467
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11715n54
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