A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565782



Internal ID16353191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100527708..100605923hg38UCSC Ensembl
Innerchr14:100994045..101072260hg19UCSC Ensembl
Innerchr14:100063798..100142013hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3878216
hg1978216
hg1878216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3898n54
Supporting Variantsnssv833076
Samples
Known GenesBEGAIN, WDR25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565782
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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