A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148378



Internal ID15654878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137478118..137708435hg38UCSC Ensembl
Innerchr9:140372570..140602887hg19UCSC Ensembl
Innerchr9:139492391..139722708hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38230318
hg19230318
hg18230318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv616023
Supporting Variants
Samples
Known GenesARRDC1, C9orf37, DPH7, EHMT1, MRPL41, PNPLA7, ZMYND19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148378
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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