A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7332



Internal ID15552331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:78796085..78840306hg38UCSC Ensembl
Outerchr10:80555842..80600063hg19UCSC Ensembl
Outerchr10:80225848..80270069hg18UCSC Ensembl
Outerchr10:80225848..80270069hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3844222
hg1944222
hg1844222
hg1744222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1904
SamplesNA18555
Known Genes
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)nsv7332
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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