A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010395



Internal ID19099612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195915037..196121393hg38UCSC Ensembl
Innerchr3:195641908..195848264hg19UCSC Ensembl
Innerchr3:197126305..197332661hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38206357
hg19206357
hg18206357
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737136
Samples
Known GenesSDHAP1, TFRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010395
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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