A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035487



Internal ID19124706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46828873..46889839hg38UCSC Ensembl
Innerchr14:47298076..47359042hg19UCSC Ensembl
Innerchr14:46367826..46428792hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3860967
hg1960967
hg1860967
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713475
Samples
Known GenesMDGA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035487
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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