A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3529830



Internal ID18481425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105563288..106209703hg38UCSC Ensembl
Innerchr14:106029625..106666346hg19UCSC Ensembl
Innerchr14:105100670..105737391hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38646416
hg19636722
hg18636722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038977
Supporting Variants
Samples
Known GenesADAM6, ELK2AP, KIAA0125, MIR8071-1, MIR8071-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3529830
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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