A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036929



Internal ID19126148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:71002431..71216695hg38UCSC Ensembl
Innerchr14:71469148..71683412hg19UCSC Ensembl
Innerchr14:70538901..70753165hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38214265
hg19214265
hg18214265
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531125
Samples
Known GenesPCNX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036929
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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