A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052837



Internal ID18795368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106364803..106877229hg38UCSC Ensembl
Innerchr14:106820732..107285437hg19UCSC Ensembl
Innerchr14:105891777..106356482hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38512427
hg19464706
hg18464706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2109n100
Supporting Variantsnssv3534009
Samples
Known GenesLINC00221
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052837
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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