A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050737



Internal ID19139956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39891162..39959504hg38UCSC Ensembl
Innerchr14:40360366..40428708hg19UCSC Ensembl
Innerchr14:39430117..39498459hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3868343
hg1968343
hg1868343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1876n100
Supporting Variantsnssv3530133, nssv3530132
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050737
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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