A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9138



Internal ID15534726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:71848127..71893350hg38UCSC Ensembl
Outerchr13:72422259..72467488hg19UCSC Ensembl
Outerchr13:71320260..71365489hg18UCSC Ensembl
Outerchr13:71320260..71365489hg17UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3845224
hg1945230
hg1845230
hg1745230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1081
Supporting Variants
SamplesNA12156
Known GenesDACH1
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)nssv9138
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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