A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703314



Internal ID15439966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98042242..98046406hg38UCSC Ensembl
Innerchr14:98508579..98512743hg19UCSC Ensembl
Innerchr14:97578332..97582496hg18UCSC Ensembl
Innerchr14:97578332..97582496hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384165
hg194165
hg184165
hg174165
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526944
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703314
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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