A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148340



Internal ID16001526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136953029..136975462hg38UCSC Ensembl
Innerchr9:139847481..139869914hg19UCSC Ensembl
Innerchr9:138967302..138989735hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3822434
hg1922434
hg1822434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615988
Supporting Variants
Samples
Known GenesLCN12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148340
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer