A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029967



Internal ID19119186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:179218100..179295043hg38UCSC Ensembl
Innerchr4:180139254..180216197hg19UCSC Ensembl
Innerchr4:180376248..180453191hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3876944
hg1976944
hg1876944
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5486n100
Supporting Variantsnssv3635561
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029967
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