A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8384



Internal ID15535480
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 StatusS
Merged Variantsnsv5782
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)nssv8384
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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