A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606432



Internal ID16047155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25948565..26183674hg38UCSC Ensembl
Innerchr7:25988185..26223294hg19UCSC Ensembl
Innerchr7:25954710..26189819hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38235110
hg19235110
hg18235110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1081144
Samples
Known GenesMIR148A, NFE2L3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606432
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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