A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565881



Internal ID16353290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101560397..101561066hg38UCSC Ensembl
Innerchr14:102026734..102027403hg19UCSC Ensembl
Innerchr14:101096487..101097156hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38670
hg19670
hg18670
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833720, nssv833722, nssv833718, nssv833724, nssv833717, nssv833723, nssv833716, nssv833721, nssv833725, nssv833719
Samples
Known GenesMIR1247
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565881
Frequency
Sample Size17421
Observed Gain4
Observed Loss6
Observed Complex0
Frequencyn/a


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