A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7736



Internal ID15552775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:36531197..36545096hg38UCSC Ensembl
Outerchr11:36552747..36566646hg19UCSC Ensembl
Outerchr11:36509323..36523222hg18UCSC Ensembl
Outerchr11:36509323..36523222hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg387133
hg197133
hg187133
hg177133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5353, nssv1932
SamplesNA18555, NA19129
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)nsv7736
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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