A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5028



Internal ID15542862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:143980552..144019546hg38UCSC Ensembl
Outerchr7:143677645..143716639hg19UCSC Ensembl
Outerchr7:143308578..143347572hg18UCSC Ensembl
Outerchr7:143115293..143154287hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3838995
hg1938995
hg1838995
hg1738995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5987
Supporting Variants
SamplesNA19129
Known GenesOR6B1
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)nssv5028
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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