A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7719



Internal ID15552756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:26146514..26200030hg38UCSC Ensembl
Outerchr11:26168061..26221577hg19UCSC Ensembl
Outerchr11:26124637..26178153hg18UCSC Ensembl
Outerchr11:26124637..26178153hg17UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg385982
hg195982
hg185982
hg175982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2860, nssv10811
SamplesNA18956, NA18555
Known Genes
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)nsv7719
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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