A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148367



Internal ID16001553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137197680..137233413hg38UCSC Ensembl
Innerchr9:140092132..140127865hg19UCSC Ensembl
Innerchr9:139211953..139247686hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3835734
hg1935734
hg1835734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv616013
Supporting Variants
Samples
Known GenesC9orf169, NDOR1, RNF208, RNF224, SLC34A3, TMEM203, TPRN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148367
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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