A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1537



Internal ID15546100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:52210049..52244870hg38UCSC Ensembl
Outerchr15:52502246..52537067hg19UCSC Ensembl
Outerchr15:50289538..50324359hg18UCSC Ensembl
Outerchr15:50289538..50324359hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3834822
hg1934822
hg1834822
hg1734822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7171
SamplesNA12156
Known GenesMYO5C
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)nsv1537
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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