A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977



Internal ID15538704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:91216313..91247509hg38UCSC Ensembl
Outerchr11:90949481..90980677hg19UCSC Ensembl
Outerchr11:90589129..90620325hg18UCSC Ensembl
Outerchr11:90589129..90620325hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg388539
hg198539
hg188539
hg178539
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv430
Supporting Variants
SamplesNA12878
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)nssv3977
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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