A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564175



Internal ID16004898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:30896678..30939804hg38UCSC Ensembl
Innerchr14:31365884..31409010hg19UCSC Ensembl
Innerchr14:30435635..30478761hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3843127
hg1943127
hg1843127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3605n54
Supporting Variantsnssv825140
Samples
Known GenesSTRN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564175
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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