A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148337



Internal ID15654837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136828956..136859658hg38UCSC Ensembl
Innerchr9:139723408..139754110hg19UCSC Ensembl
Innerchr9:138843229..138873931hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3830703
hg1930703
hg1830703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615985
Supporting Variants
Samples
Known GenesC9orf172, MAMDC4, MIR4292, PHPT1, RABL6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148337
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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