A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv990225



Internal ID16284181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6782340..6783611hg38UCSC Ensembl
Innerchr4:6784067..6785338hg19UCSC Ensembl
Innerchr4:6834968..6836239hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381272
hg191272
hg181272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593530
Supporting Variants
Samples
Known GenesKIAA0232
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv990225
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