A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483120



Internal ID15582233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83591137..83738257hg38UCSC Ensembl
Innerchr7:83220453..83367573hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38147121
hg19147121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996140
Samples
Known GenesMIR7976, SEMA3E
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483120
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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