A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10189



Internal ID15195923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:109676612..109713180hg38UCSC Ensembl
Outerchr1:110219234..110255802hg19UCSC Ensembl
Outerchr1:110020757..110057325hg18UCSC Ensembl
Outerchr1:109931276..109967844hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3836569
hg1936569
hg1836569
hg1736569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2310
Supporting Variants
SamplesNA18956
Known GenesGSTM1, GSTM2, GSTM5
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)nssv10189
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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