A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6977



Internal ID15205254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:67945718..67979446hg38UCSC Ensembl
Outerchr10:69705475..69739203hg19UCSC Ensembl
Outerchr10:69375481..69409209hg18UCSC Ensembl
Outerchr10:69375481..69409209hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg386022
hg196022
hg186022
hg176022
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3880
SamplesNA12878
Known GenesHERC4
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)nsv6977
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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