A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000173



Internal ID19089390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:100006845..100043247hg38UCSC Ensembl
Innerchr4:100928002..100964404hg19UCSC Ensembl
Innerchr4:101147025..101183427hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3836403
hg1936403
hg1836403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3742898
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)nsv1000173
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