A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041194



Internal ID19130413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85386736..85430208hg38UCSC Ensembl
Innerchr14:85853080..85896552hg19UCSC Ensembl
Innerchr14:84922833..84966305hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3843473
hg1943473
hg1843473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1949n100
Supporting Variantsnssv3713540
Samples
Known GenesLINC00911
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041194
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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