A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10149



Internal ID15542649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:14803425..14829490hg38UCSC Ensembl
Outerchr18:14803424..14829489hg19UCSC Ensembl
Outerchr18:14793424..14819489hg18UCSC Ensembl
Outerchr18:14793424..14819489hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3826066
hg1926066
hg1826066
hg1726066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2216
Supporting Variants
SamplesNA18956
Known GenesANKRD30B
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)nssv10149
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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