A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1576



Internal ID15546139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:67677642..67722735hg38UCSC Ensembl
Outerchr15:67969980..68015073hg19UCSC Ensembl
Outerchr15:65757034..65802127hg18UCSC Ensembl
Outerchr15:65757034..65802127hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3845094
hg1945094
hg1845094
hg1745094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7190
SamplesNA12156
Known GenesMAP2K5
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)nsv1576
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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