A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3888



Internal ID15191929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:93316110..93351114hg38UCSC Ensembl
Outerchr10:95075867..95110871hg19UCSC Ensembl
Outerchr10:95065857..95100861hg18UCSC Ensembl
Outerchr10:95065857..95100861hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg384744
hg194744
hg184744
hg174744
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7494
Supporting Variants
SamplesNA12878
Known GenesMYOF
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)nssv3888
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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