A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996334



Internal ID15235194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34865867..35052633hg38UCSC Ensembl
Innerchr14:35335073..35521839hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38186767
hg19186767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483012
Supporting Variants
Samples
Known GenesBAZ1A, FAM177A1, IGBP1P1, SRP54
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996334
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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