A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001354



Internal ID19090571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665110..94686257hg38UCSC Ensembl
Innerchr1:95130666..95151813hg19UCSC Ensembl
Innerchr1:94903254..94924401hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3821148
hg1921148
hg1821148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv208n100
Supporting Variantsnssv3469714, nssv3477828
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)nsv1001354
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer