A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5818



Internal ID15550665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:84245652..84290488hg38UCSC Ensembl
Outerchr7:83874968..83919804hg19UCSC Ensembl
Outerchr7:83712904..83757740hg18UCSC Ensembl
Outerchr7:83519619..83564455hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3844837
hg1944837
hg1844837
hg1744837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8392
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)nsv5818
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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