A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2817690



Internal ID15683901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30313721..30383419hg38UCSC Ensembl
Innerchr15:30605924..30675622hg19UCSC Ensembl
Innerchr15:28393216..28462914hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3869699
hg1969699
hg1869699
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514775
Supporting Variants
SamplesNA18603
Known GenesCHRFAM7A
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2817690
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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