A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6724



Internal ID15204976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:128823206..128858415hg38UCSC Ensembl
Outerchr9:131585485..131620694hg19UCSC Ensembl
Outerchr9:130625306..130660515hg18UCSC Ensembl
Outerchr9:128665039..128700248hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg385792
hg195792
hg185792
hg175792
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv838
SamplesNA19240
Known GenesC9orf114, CCBL1
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)nsv6724
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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