A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7177



Internal ID15190001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:59981619..60021111hg38UCSC Ensembl
Outerchr15:60273818..60313310hg19UCSC Ensembl
Outerchr15:58061110..58100602hg18UCSC Ensembl
Outerchr15:58061110..58100602hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3839493
hg1939493
hg1839493
hg1739493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1554
Supporting Variants
SamplesNA12156
Known GenesFOXB1
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)nssv7177
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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