A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054995



Internal ID19144214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:37608822..37668971hg38UCSC Ensembl
Innerchr14:38078027..38138176hg19UCSC Ensembl
Innerchr14:37147778..37207927hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3860150
hg1960150
hg1860150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528629
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)nsv1054995
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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