A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607850



Internal ID16395259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:93908763..93913138hg38UCSC Ensembl
Innerchr7:93538075..93542450hg19UCSC Ensembl
Innerchr7:93376011..93380386hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg384376
hg194376
hg184376
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1090589
Samples
Known GenesGNGT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607850
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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