A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9355n54



Internal ID22777250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:161093011..161169603hg38UCSC Ensembl
chr4:162014163..162090755hg19UCSC Ensembl
chr4:162233613..162310205hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3876593
hg1976593
hg1876593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv595942, nsv595943, nsv595944
Samples1780854179_A, NINDS_180
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9355n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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