A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023204



Internal ID19112421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:109157344..109290856hg38UCSC Ensembl
Innerchr8:110169573..110303085hg19UCSC Ensembl
Innerchr8:110238749..110372261hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38133513
hg19133513
hg18133513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7281n100
Supporting Variantsnssv3691272, nssv3691273, nssv3757337
Samples
Known GenesNUDCD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023204
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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