A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148282



Internal ID16001468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135907024..135908168hg38UCSC Ensembl
Innerchr9:138798870..138800014hg19UCSC Ensembl
Innerchr9:137938691..137939835hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381145
hg191145
hg181145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615941
Supporting Variants
Samples
Known GenesCAMSAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148282
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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