A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008236



Internal ID19097455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:118068312..118232869hg38UCSC Ensembl
Innerchr4:118989467..119154024hg19UCSC Ensembl
Innerchr4:119208915..119373472hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38164558
hg19164558
hg18164558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639340
Samples
Known GenesNDST3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008236
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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