A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6730



Internal ID15551669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:130134004..130168596hg38UCSC Ensembl
Outerchr9:132896283..132930875hg19UCSC Ensembl
Outerchr9:131936104..131970696hg18UCSC Ensembl
Outerchr9:129975837..130010429hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386400
hg196400
hg186400
hg176400
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv840
SamplesNA19240
Known GenesGPR107
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)nsv6730
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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