A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867



Internal ID15550719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:100169151..100202132hg38UCSC Ensembl
Outerchr7:99766774..99799755hg19UCSC Ensembl
Outerchr7:99604710..99637691hg18UCSC Ensembl
Outerchr7:99411425..99444406hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3832982
hg1932982
hg1832982
hg1732982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6153
SamplesNA12156
Known GenesGATS, GPC2, STAG3
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)nsv5867
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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