A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3665



Internal ID15548297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:49675926..49708887hg38UCSC Ensembl
Outerchr22:50069574..50102535hg19UCSC Ensembl
Outerchr22:48455578..48488539hg18UCSC Ensembl
Outerchr22:48390435..48423396hg17UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg386476
hg196476
hg186476
hg176476
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6990
SamplesNA12156
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)nsv3665
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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