A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998152



Internal ID19157689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1696467..1756236hg38UCSC Ensembl
Innerchr1:1627906..1687675hg19UCSC Ensembl
Innerchr1:1617766..1677535hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3859770
hg1959770
hg1859770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9n100
Supporting Variantsnssv3481980, nssv3464349
Samples
Known GenesCDK11A, CDK11B, MMP23A, NADK, SLC35E2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998152
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