A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1912



Internal ID15541195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122591027..122621213hg38UCSC Ensembl
Outerchr10:124350543..124380729hg19UCSC Ensembl
Outerchr10:124340533..124370719hg18UCSC Ensembl
Outerchr10:124340533..124370719hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3830187
hg1930187
hg1830187
hg1730187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7581
Supporting Variants
SamplesNA18555
Known GenesDMBT1
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)nssv1912
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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