A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10802



Internal ID15195310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:10532842..10565476hg38UCSC Ensembl
Outerchr11:10554389..10587023hg19UCSC Ensembl
Outerchr11:10510965..10543599hg18UCSC Ensembl
Outerchr11:10510965..10543599hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg386875
hg196875
hg186875
hg176875
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7675
Supporting Variants
SamplesNA18956
Known GenesLYVE1, MRVI1-AS1, RNF141
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)nssv10802
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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