A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615526



Internal ID16056249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130491981..130520222hg38UCSC Ensembl
Innerchr9:133367368..133395609hg19UCSC Ensembl
Innerchr9:132357189..132385430hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3828242
hg1928242
hg1828242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12911n54
Supporting Variantsnssv1176511
SamplesNINDS_70
Known GenesASS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615526
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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