A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614788



Internal ID16055511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87801061..88227679hg38UCSC Ensembl
Innerchr9:90415976..90842594hg19UCSC Ensembl
Innerchr9:89605796..90032414hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38426619
hg19426619
hg18426619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139086
Samples
Known GenesCDK20, CTSLP8, LOC392364, SPATA31C1, SPATA31C2, SPATA31E1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614788
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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