A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2995908



Internal ID15234768
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 StatusS
Merged Variantsnsv483005
Supporting Variants
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)nssv2995908
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer