A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9937



Internal ID15193339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:996222..1019734hg38UCSC Ensembl
Outerchr11:996222..1019734hg19UCSC Ensembl
Outerchr11:986222..1009734hg18UCSC Ensembl
Outerchr11:986222..1009734hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3810304
hg1910304
hg1810304
hg1710304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7637
Supporting Variants
SamplesNA18507
Known GenesAP2A2, MUC6
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)nssv9937
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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