A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483005



Internal ID15235479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44530751..44705087hg38UCSC Ensembl
Innerchr19:45034773..45208356hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38174337
hg19173584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996266, nssv2995908
Samples
Known GenesCEACAM16, CEACAM19, CEACAM22P, IGSF23, MIR4531, PVR
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483005
Frequency
Sample Size39
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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