A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6643



Internal ID15204887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46040213..46075212hg38UCSC Ensembl
Outerchr10:51520610..51555609hg19UCSC Ensembl
Outerchr10:51190616..51225615hg18UCSC Ensembl
Outerchr10:51190616..51225615hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg384749
hg194749
hg184749
hg174749
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3878
SamplesNA12878
Known GenesMSMB
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)nsv6643
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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