A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561



Internal ID8518465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:73140727..73175683hg38UCSC Ensembl
Outerchr9:75755643..75790599hg19UCSC Ensembl
Outerchr9:74945463..74980419hg18UCSC Ensembl
Outerchr9:72985197..73020153hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg386032
hg196032
hg186032
hg176032
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv809
SamplesNA19240
Known GenesANXA1
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)nsv6561
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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