A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5782



Internal ID15550626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:69481897..69526918hg38UCSC Ensembl
Outerchr7:68946883..68991904hg19UCSC Ensembl
Outerchr7:68584819..68629840hg18UCSC Ensembl
Outerchr7:68391534..68436555hg17UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3845022
hg1945022
hg1845022
hg1745022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8384
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)nsv5782
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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