A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608421



Internal ID16049144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:130722761..130784338hg38UCSC Ensembl
Innerchr7:130407589..130469097hg19UCSC Ensembl
Innerchr7:130058129..130119637hg18UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3861578
hg1961509
hg1861509
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1094520
Samples
Known GenesKLF14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608421
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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