A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913



Internal ID15204084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:114546846..114579372hg38UCSC Ensembl
Outerchr7:114186901..114219427hg19UCSC Ensembl
Outerchr7:113974137..114006663hg18UCSC Ensembl
Outerchr7:113780852..113813378hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg387218
hg197218
hg187218
hg177218
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570
SamplesNA12878
Known GenesFOXP2
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)nsv5913
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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