A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998228



Internal ID19157765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194885911..194921887hg38UCSC Ensembl
Innerchr3:194606640..194642616hg19UCSC Ensembl
Innerchr3:196087929..196123905hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3835977
hg1935977
hg1835977
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3611376, nssv3611377
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998228
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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