A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1094785



Internal ID15947971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135434669..135798303hg38UCSC Ensembl
Innerchr7:135119417..135483051hg19UCSC Ensembl
Innerchr7:134769957..135133591hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38363635
hg19363635
hg18363635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608460
Supporting Variants
Samples
Known GenesC7orf73, CNOT4, FAM180A, NUP205, SLC13A4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1094785
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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