A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697552



Internal ID18649147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92295180..92376282hg38UCSC Ensembl
Innerchr9:95057462..95138564hg19UCSC Ensembl
Innerchr9:94097283..94178385hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3881103
hg1981103
hg1881103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045165
Supporting Variants
Samples
Known GenesCENPP, NOL8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697552
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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