A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148361



Internal ID15654861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137079368..137240666hg38UCSC Ensembl
Innerchr9:139973820..140135118hg19UCSC Ensembl
Innerchr9:139093641..139254939hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38161299
hg19161299
hg18161299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv616007
Supporting Variants
Samples
Known GenesANAPC2, C9orf169, DPP7, GRIN1, LRRC26, MAN1B1, MAN1B1-AS1, MIR3621, NDOR1, RNF208, RNF224, SLC34A3, SSNA1, TMEM203, TMEM210, TPRN, UAP1L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148361
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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