A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021859



Internal ID19111077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34547659..34567512hg38UCSC Ensembl
Innerchr6:34515436..34535289hg19UCSC Ensembl
Innerchr6:34623414..34643267hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3819854
hg1919854
hg1819854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657368
Samples
Known GenesSPDEF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021859
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