A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608459



Internal ID16395868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135332283..135353636hg38UCSC Ensembl
Innerchr7:135017035..135038388hg19UCSC Ensembl
Innerchr7:134667575..134688928hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3821354
hg1921354
hg1821354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155236
SamplesNINDS_98
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608459
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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