A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696406



Internal ID18648001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132923184..132937614hg38UCSC Ensembl
Innerchr9:135798571..135813001hg19UCSC Ensembl
Innerchr9:134788392..134802822hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3814431
hg1914431
hg1814431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038328
Supporting Variants
Samples
Known GenesTSC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696406
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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