A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5674



Internal ID15197070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:75172907..75196796hg38UCSC Ensembl
Outerchr17:73169002..73192891hg19UCSC Ensembl
Outerchr17:70680597..70704486hg18UCSC Ensembl
Outerchr17:70680597..70704486hg17UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3823890
hg1923890
hg1823890
hg1723890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2141
Supporting Variants
SamplesNA19129
Known GenesSUMO2
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)nssv5674
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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