A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036815



Internal ID19126034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:45488399..45582425hg38UCSC Ensembl
Innerchr14:45957602..46051628hg19UCSC Ensembl
Innerchr14:45027352..45121378hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3894027
hg1994027
hg1894027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713467
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)nsv1036815
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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