A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6620



Internal ID15204862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:48989299..49016590hg38UCSC Ensembl
Outerchr10:50197344..50224635hg19UCSC Ensembl
Outerchr10:49867350..49894641hg18UCSC Ensembl
Outerchr10:49867350..49894641hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3827292
hg1927292
hg1827292
hg1727292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv910
SamplesNA19240
Known GenesVSTM4
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)nsv6620
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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