A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998955



Internal ID19158491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:183722969..183795597hg38UCSC Ensembl
Innerchr3:183440757..183513385hg19UCSC Ensembl
Innerchr3:184923451..184996079hg18UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3872629
hg1972629
hg1872629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3615003
Samples
Known GenesYEATS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998955
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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