A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614221



Internal ID16401630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38067633..38069476hg38UCSC Ensembl
Innerchr9:38067630..38069473hg19UCSC Ensembl
Innerchr9:38057630..38059473hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg381844
hg191844
hg181844
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1133976
Samples
Known GenesSHB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614221
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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