A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038633



Internal ID19127852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43765759..44431855hg38UCSC Ensembl
Innerchr14:44234962..44901058hg19UCSC Ensembl
Innerchr14:43304712..43970808hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38666097
hg19666097
hg18666097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1894n100
Supporting Variantsnssv3530271
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)nsv1038633
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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