A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7211



Internal ID15536653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:87041346..87066767hg38UCSC Ensembl
Outerchr15:87584577..87609998hg19UCSC Ensembl
Outerchr15:85385581..85411002hg18UCSC Ensembl
Outerchr15:85385581..85411002hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3825422
hg1925422
hg1825422
hg1725422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1649
Supporting Variants
SamplesNA12156
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)nssv7211
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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