A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1094784



Internal ID15601284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135016632..135149118hg38UCSC Ensembl
Innerchr7:134701383..134833870hg19UCSC Ensembl
Innerchr7:134351923..134484410hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38132487
hg19132488
hg18132488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608458
Supporting Variants
Samples
Known GenesAGBL3, TMEM140
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1094784
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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