A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616994



Internal ID18568589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196124925..196411200hg38UCSC Ensembl
Innerchr3:195851796..196138071hg19UCSC Ensembl
Innerchr3:197336193..197622468hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38286276
hg19286276
hg18286276
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009811
Supporting Variants
Samples
Known GenesLINC00885, PCYT1A, SLC51A, TCTEX1D2, TM4SF19, TM4SF19-TCTEX1D2, UBXN7, ZDHHC19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616994
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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