A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007607



Internal ID19096826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:134412679..134437972hg38UCSC Ensembl
Innerchr3:134131521..134156814hg19UCSC Ensembl
Innerchr3:135614211..135639504hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3825294
hg1925294
hg1825294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3607145
Samples
Known GenesMIR4788
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007607
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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