A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527606



Internal ID15454899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100051488..100066865hg38UCSC Ensembl
Innerchr14:100517825..100533202hg19UCSC Ensembl
Innerchr14:99587578..99602955hg18UCSC Ensembl
Innerchr14:99587578..99602955hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3815378
hg1915378
hg1815378
hg1715378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv142n21
Supporting Variantsnssv704068
Samples
Known GenesEVL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527606
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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