A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1025297



Internal ID16319253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:11782530..11822721hg38UCSC Ensembl
Innerchr5:11782642..11822833hg19UCSC Ensembl
Innerchr5:11835642..11875833hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3840192
hg1940192
hg1840192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597154
Supporting Variants
Samples
Known GenesCTNND2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1025297
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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