A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587



Internal ID15204825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:48318286..48363761hg38UCSC Ensembl
Outerchr10:49526329..49571804hg19UCSC Ensembl
Outerchr10:49196335..49241810hg18UCSC Ensembl
Outerchr10:49196335..49241810hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3845476
hg1945476
hg1845476
hg1745476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6397
SamplesNA12156
Known GenesMAPK8
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)nsv6587
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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