A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609



Internal ID15204849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:48562374..48570165hg38UCSC Ensembl
Outerchr10:49770419..49778210hg19UCSC Ensembl
Outerchr10:49440425..49448216hg18UCSC Ensembl
Outerchr10:49440425..49448216hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg387792
hg197792
hg187792
hg177792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8685
SamplesNA12156
Known GenesARHGAP22
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)nsv6609
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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