A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002928



Internal ID19092145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94660980..94687282hg38UCSC Ensembl
Innerchr1:95126536..95152838hg19UCSC Ensembl
Innerchr1:94899124..94925426hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3826303
hg1926303
hg1826303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv208n100
Supporting Variantsnssv3468312
Samples
Known GenesLINC01057
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002928
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