A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614157



Internal ID16054880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34695472..34737831hg38UCSC Ensembl
Innerchr9:34695469..34737828hg19UCSC Ensembl
Innerchr9:34685469..34727828hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3842360
hg1942360
hg1842360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132849
Samples
Known GenesCCL21, FAM205A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614157
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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