A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022751



Internal ID19111969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22620751..22674271hg38UCSC Ensembl
Innerchr9:22620750..22674270hg19UCSC Ensembl
Innerchr9:22610750..22664270hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3853521
hg1953521
hg1853521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755837
Samples
Known GenesFLJ35282
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022751
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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