A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6210



Internal ID15204411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:29481156..29503058hg38UCSC Ensembl
Outerchr10:29770085..29791987hg19UCSC Ensembl
Outerchr10:29810091..29831993hg18UCSC Ensembl
Outerchr10:29810091..29831993hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3821903
hg1921903
hg1821903
hg1721903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8537
SamplesNA12156
Known GenesSVIL
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)nsv6210
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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