A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013700



Internal ID19102919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665110..94689831hg38UCSC Ensembl
Innerchr1:95130666..95155387hg19UCSC Ensembl
Innerchr1:94903254..94927975hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3824722
hg1924722
hg1824722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv208n100
Supporting Variantsnssv3479541, nssv3470294, nssv3467106, nssv3478150, nssv3465073
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)nsv1013700
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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