A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9145



Internal ID15534719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:88835323..88880550hg38UCSC Ensembl
Outerchr13:89487577..89532804hg19UCSC Ensembl
Outerchr13:88285578..88330805hg18UCSC Ensembl
Outerchr13:88285578..88330805hg17UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3845228
hg1945228
hg1845228
hg1745228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114
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)nssv9145
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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