A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020637



Internal ID19109856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90688742..90857507hg38UCSC Ensembl
Innerchr7:90318056..90486822hg19UCSC Ensembl
Innerchr7:90155992..90324758hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38168766
hg19168767
hg18168767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655237, nssv3655239, nssv3655238
Samples
Known GenesCDK14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020637
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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