A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7648



Internal ID15552678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:2945067..2976295hg38UCSC Ensembl
Outerchr11:2966297..2997525hg19UCSC Ensembl
Outerchr11:2922873..2954101hg18UCSC Ensembl
Outerchr11:2922873..2954101hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388209
hg198209
hg188209
hg178209
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6438
SamplesNA12156
Known GenesNAP1L4, SNORA54
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)nsv7648
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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