A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996195



Internal ID15581696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:90697247..90847497hg38UCSC Ensembl
Innerchr4:91618398..91768648hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38150251
hg19150251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483045
Supporting Variants
Samples
Known GenesCCSER1
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996195
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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