A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515152



Internal ID15813511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76507400..76510224hg38UCSC Ensembl
Innerchr9:79122316..79125140hg19UCSC Ensembl
Innerchr9:78312136..78314960hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382825
hg192825
hg182825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2975449, nssv2975448, nssv2975450, nssv2975447
SamplesNA12751, NA07048, NA07055, NA12740
Known GenesGCNT1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv515152
Frequency
Sample Size2366
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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