A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8075



Internal ID15535789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:16681057..16707248hg38UCSC Ensembl
Outerchr5:16681166..16707357hg19UCSC Ensembl
Outerchr5:16734166..16760357hg18UCSC Ensembl
Outerchr5:16734166..16760357hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3826192
hg1926192
hg1826192
hg1726192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737
Supporting Variants
SamplesNA12156
Known GenesMYO10
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)nssv8075
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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