A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6221



Internal ID15204423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:29494894..29528303hg38UCSC Ensembl
Outerchr10:29783823..29817232hg19UCSC Ensembl
Outerchr10:29823829..29857238hg18UCSC Ensembl
Outerchr10:29823829..29857238hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg386026
hg196026
hg186026
hg176026
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8546
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)nsv6221
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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