A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029709



Internal ID19118928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158258641..158592892hg38UCSC Ensembl
Innerchr7:158051333..158385584hg19UCSC Ensembl
Innerchr7:157744094..158078345hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38334252
hg19334252
hg18334252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674737
Samples
Known GenesMIR5707, MIR595, PTPRN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029709
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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