A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003711



Internal ID19092929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102190625..102378068hg38UCSC Ensembl
Innerchr1:102656181..102843624hg19UCSC Ensembl
Innerchr1:102428769..102616212hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38187444
hg19187444
hg18187444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv210n100
Supporting Variantsnssv3466542
Samples
Known GenesMIR548AI
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003711
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