A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3474438



Internal ID19065977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665110..94689978hg38UCSC Ensembl
Innerchr1:95130666..95155534hg19UCSC Ensembl
Innerchr1:94903254..94928122hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3824869
hg1924869
hg1824869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012925
Supporting Variants
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)nssv3474438
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