A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141032



Internal ID15994218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:108395901..108434101hg38UCSC Ensembl
Innerchr9:111158181..111196381hg19UCSC Ensembl
Innerchr9:110198002..110236202hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3838201
hg1938201
hg1838201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615144
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141032
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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