A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009536



Internal ID19098754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176940347..177167118hg38UCSC Ensembl
Innerchr3:176658135..176884906hg19UCSC Ensembl
Innerchr3:178140829..178367600hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38226772
hg19226772
hg18226772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4996n100
Supporting Variantsnssv3614959
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)nsv1009536
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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