A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7635



Internal ID15205978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:954928..958292hg38UCSC Ensembl
Outerchr11:954928..958292hg19UCSC Ensembl
Outerchr11:944928..948292hg18UCSC Ensembl
Outerchr11:944928..948292hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg386588
hg196588
hg186588
hg176588
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10788
SamplesNA18956
Known GenesAP2A2
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv7635
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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