A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6633



Internal ID15537230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:54904232..54942913hg38UCSC Ensembl
Outerchr15:55196430..55235111hg19UCSC Ensembl
Outerchr15:52983722..53022403hg18UCSC Ensembl
Outerchr15:52983722..53022403hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3838682
hg1938682
hg1838682
hg1738682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1541
Supporting Variants
SamplesNA12156
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)nssv6633
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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