A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996244



Internal ID15235104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:126448508..126598884hg38UCSC Ensembl
InnerchrX:125582491..125732867hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38150377
hg19150377
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483075
Supporting Variants
Samples
Known GenesDCAF12L1
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996244
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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