A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148375



Internal ID15654875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137229132..137338927hg38UCSC Ensembl
Innerchr9:140123584..140233379hg19UCSC Ensembl
Innerchr9:139243405..139353200hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38109796
hg19109796
hg18109796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv616020
Supporting Variants
Samples
Known GenesC9orf173, EXD3, FAM166A, LOC100129722, NELFB, NRARP, RNF224, SLC34A3, TOR4A, TUBB4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148375
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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