A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515150



Internal ID15466784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69483656..69505504hg38UCSC Ensembl
Innerchr9:72098572..72120420hg19UCSC Ensembl
Innerchr9:71288392..71310240hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3821849
hg1921849
hg1821849
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2975406, nssv2975400, nssv2975399, nssv2975392, nssv2975403, nssv2975395, nssv2975397, nssv2975405, nssv2975404, nssv2975407, nssv2975401, nssv2975402, nssv2975398, nssv2975394, nssv2975393, nssv2975396
SamplesNA10831, NA18863, NA21524, NA18952, NA18953, NA18862, NA19140, NA11994, NA12155, NA21525, NA21648, NA18910, NA19235, NA21635, NA12248, NA21526
Known GenesAPBA1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv515150
Frequency
Sample Size2366
Observed Gain8
Observed Loss8
Observed Complex0
Frequencyn/a


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