A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684711



Internal ID15074677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105585696..105733242hg38UCSC Ensembl
Innerchr14:106052033..106199579hg19UCSC Ensembl
Innerchr14:105123078..105270624hg18UCSC Ensembl
Innerchr14:105123078..105270624hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38147547
hg19147547
hg18147547
hg17147547
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517055
Supporting Variants
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684711
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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