A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615641



Internal ID16403050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133660184..133668909hg38UCSC Ensembl
Innerchr9:136525306..136534031hg19UCSC Ensembl
Innerchr9:135515127..135523852hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg388726
hg198726
hg188726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1145449
Samples
Known GenesSARDH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615641
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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