A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv986888



Internal ID15934158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196132016..196345571hg38UCSC Ensembl
Innerchr3:195858887..196072442hg19UCSC Ensembl
Innerchr3:197343284..197556839hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38213556
hg19213556
hg18213556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593071
Supporting Variants
Samples
Known GenesLINC00885, PCYT1A, SLC51A, TCTEX1D2, TM4SF19, TM4SF19-TCTEX1D2, ZDHHC19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv986888
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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