A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1580



Internal ID15546143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68113325..68138410hg38UCSC Ensembl
Outerchr15:68405663..68430748hg19UCSC Ensembl
Outerchr15:66192717..66217802hg18UCSC Ensembl
Outerchr15:66192717..66217802hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3825086
hg1925086
hg1825086
hg1725086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2111
SamplesNA18555
Known GenesPIAS1
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)nsv1580
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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