A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11570n54



Internal ID20144994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:110662639..110702956hg38UCSC Ensembl
chr7:110302695..110343012hg19UCSC Ensembl
chr7:110089931..110130248hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3840318
hg1940318
hg1840318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608148, nsv608149
SamplesNINDS_208
Known GenesIMMP2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11570n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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