A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532571



Internal ID18484166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:87932062..87953014hg38UCSC Ensembl
Innerchr14:88398406..88419358hg19UCSC Ensembl
Innerchr14:87468159..87489111hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3820953
hg1920953
hg1820953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036923
Supporting Variants
Samples
Known GenesGALC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3532571
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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