A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014824



Internal ID19104041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176940347..177161217hg38UCSC Ensembl
Innerchr3:176658135..176879005hg19UCSC Ensembl
Innerchr3:178140829..178361699hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38220871
hg19220871
hg18220871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4996n100
Supporting Variantsnssv3738451
Samples
Known GenesTBL1XR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014824
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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