A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148341



Internal ID15654841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136966179..137147868hg38UCSC Ensembl
Innerchr9:139860631..140042320hg19UCSC Ensembl
Innerchr9:138980452..139162141hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38181690
hg19181690
hg18181690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615989
Supporting Variants
Samples
Known GenesABCA2, C9orf139, C9orf142, CLIC3, DPP7, ENTPD2, FUT7, GRIN1, LCNL1, MAN1B1, MAN1B1-AS1, NPDC1, PTGDS, SAPCD2, UAP1L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148341
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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