A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025861



Internal ID19115078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:9805807..9948761hg38UCSC Ensembl
Innerchr6:9806040..9948994hg19UCSC Ensembl
Innerchr6:9914026..10056980hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38142955
hg19142955
hg18142955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5916n100
Supporting Variantsnssv3654760
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)nsv1025861
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