A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022697



Internal ID18765231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18951532..19010896hg38UCSC Ensembl
Innerchr9:18951530..19010894hg19UCSC Ensembl
Innerchr9:18941530..19000894hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3859365
hg1959365
hg1859365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755827
Samples
Known GenesFAM154A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022697
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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