A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7221



Internal ID15536643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:100515110..100553555hg38UCSC Ensembl
Outerchr15:101055315..101093760hg19UCSC Ensembl
Outerchr15:98872838..98911283hg18UCSC Ensembl
Outerchr15:98872838..98911283hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3838446
hg1938446
hg1838446
hg1738446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1690
Supporting Variants
SamplesNA12156
Known GenesCERS3, PRKXP1
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)nssv7221
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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