A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565516



Internal ID16006239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:90508674..90561264hg38UCSC Ensembl
Innerchr14:90975018..91027608hg19UCSC Ensembl
Innerchr14:90044771..90097361hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3852591
hg1952591
hg1852591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149535
Samples1780862019_A
Known GenesTTC7B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565516
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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