A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615980



Internal ID16056703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136624513..136696482hg38UCSC Ensembl
Innerchr9:139518965..139590934hg19UCSC Ensembl
Innerchr9:138638786..138710755hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3871970
hg1971970
hg1871970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv13005n54
Supporting Variantsnssv1148334
Samples
Known GenesAGPAT2, EGFL7, MIR126
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615980
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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