A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2109



Internal ID15194706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:58122615..58155766hg38UCSC Ensembl
Outerchr15:58414814..58447965hg19UCSC Ensembl
Outerchr15:56202106..56235257hg18UCSC Ensembl
Outerchr15:56202106..56235257hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386839
hg196839
hg186839
hg176839
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1549
Supporting Variants
SamplesNA18555
Known GenesAQP9
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)nssv2109
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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