A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615534



Internal ID16056257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130894835..130934388hg38UCSC Ensembl
Innerchr9:133770222..133809775hg19UCSC Ensembl
Innerchr9:132760043..132799596hg18UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg3839554
hg1939554
hg1839554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176512
SamplesNINDS_271
Known GenesFIBCD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615534
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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