A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038977



Internal ID18781508
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 StatusM
Merged Variantsdgv1985n100
Supporting Variantsnssv3529830
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)nsv1038977
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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