A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516770



Internal ID15444063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:68738151..68743342hg38UCSC Ensembl
Innerchr14:69204868..69210059hg19UCSC Ensembl
Innerchr14:68274621..68279812hg18UCSC Ensembl
Innerchr14:68274621..68279812hg17UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg385192
hg195192
hg185192
hg175192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685532, nssv670853, nssv670733, nssv683016, nssv662422
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516770
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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