A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148256



Internal ID15654756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135903671..135992854hg38UCSC Ensembl
Innerchr9:138795517..138884700hg19UCSC Ensembl
Innerchr9:137935338..138024521hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3889184
hg1989184
hg1889184
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615929
Supporting Variants
Samples
Known GenesCAMSAP1, UBAC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148256
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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