A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7650



Internal ID15552681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3372740..3383537hg38UCSC Ensembl
Outerchr11:3393970..3404767hg19UCSC Ensembl
Outerchr11:3350546..3361343hg18UCSC Ensembl
Outerchr11:3350546..3361343hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387188
hg197188
hg187188
hg177188
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2856
SamplesNA18555
Known GenesLOC650368, ZNF195
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)nsv7650
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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