A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565453



Internal ID16352862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85960618..86033755hg38UCSC Ensembl
Innerchr14:86426962..86500099hg19UCSC Ensembl
Innerchr14:85496715..85569852hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3873138
hg1973138
hg1873138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3831n54
Supporting Variantsnssv832009, nssv832008, nssv1149509
Samples1780854459_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565453
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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