A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5574



Internal ID15543876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:91648396..91693178hg38UCSC Ensembl
Outerchr15:92191626..92236408hg19UCSC Ensembl
Outerchr15:89992630..90037412hg18UCSC Ensembl
Outerchr15:89992630..90037412hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3844783
hg1944783
hg1844783
hg1744783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1664
Supporting Variants
SamplesNA19129
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)nssv5574
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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