A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1959



Internal ID15546522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:6122932..6153253hg38UCSC Ensembl
Outerchr17:6026252..6056573hg19UCSC Ensembl
Outerchr17:5966976..5997297hg18UCSC Ensembl
Outerchr17:5966976..5997297hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3830322
hg1930322
hg1830322
hg1730322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7302
SamplesNA12156
Known GenesWSCD1
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)nsv1959
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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