A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565575



Internal ID16352984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93241878..93246700hg38UCSC Ensembl
Innerchr14:93708224..93713046hg19UCSC Ensembl
Innerchr14:92777977..92782799hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg384823
hg194823
hg184823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832436
Samples
Known GenesBTBD7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565575
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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