A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2995917



Internal ID15234777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100674835..100852920hg38UCSC Ensembl
Innerchr14:101141172..101319257hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38178086
hg19178086
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483116
Supporting Variants
Samples
Known GenesDLK1, MEG3, MIR2392, MIR770
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2995917
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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