A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507



Internal ID15550323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:141709688..141733549hg38UCSC Ensembl
Outerchr6:142030825..142054686hg19UCSC Ensembl
Outerchr6:142072518..142096379hg18UCSC Ensembl
Outerchr6:142072518..142096379hg17UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3823862
hg1923862
hg1823862
hg1723862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9895
SamplesNA18507
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)nsv5507
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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