A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038085



Internal ID19127304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27287258..27374103hg38UCSC Ensembl
Innerchr14:27756464..27843309hg19UCSC Ensembl
Innerchr14:26826304..26913149hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3886846
hg1986846
hg1886846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1858n100
Supporting Variantsnssv3528563
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)nsv1038085
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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