A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012627



Internal ID19101844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38235456..38261648hg38UCSC Ensembl
Innerchr4:38237077..38263269hg19UCSC Ensembl
Innerchr4:37913472..37939664hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3826193
hg1926193
hg1826193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625030
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)nsv1012627
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