A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451736



Internal ID18621610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62798833..62958371hg38UCSC Ensembl
Innerchr9:66454657..66614195hg19UCSC Ensembl
Innerchr9:66194477..66354015hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38159539
hg19159539
hg18159539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428216
Supporting Variants
SamplesNA19113
Known GenesMGC21881, PTGER4P2-CDK2AP2P2
MethodBAC aCGH
AnalysisCopy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006).
PlatformSanger H. sapiens Whole Genome Tile Path 28.7k v3
Comments
ReferencePerry_et_al_2008b
Pubmed ID18775914
Accession Number(s)nssv451736
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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