A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1341



Internal ID15544376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:6944886..6980654hg38UCSC Ensembl
Outerchr17:6848205..6883973hg19UCSC Ensembl
Outerchr17:6788929..6824697hg18UCSC Ensembl
Outerchr17:6788929..6824697hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3835769
hg1935769
hg1835769
hg1735769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1961
Supporting Variants
SamplesNA19240
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)nssv1341
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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