A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817



Internal ID15544694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:88508189..88543070hg38UCSC Ensembl
Outerchr9:91123104..91157985hg19UCSC Ensembl
Outerchr9:90312924..90347805hg18UCSC Ensembl
Outerchr9:88352658..88387539hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg386116
hg196116
hg186116
hg176116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605
Supporting Variants
SamplesNA19240
Known GenesNXNL2
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)nssv817
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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