A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8810



Internal ID15535054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:71106349..71124312hg38UCSC Ensembl
Outerchr10:72866106..72884069hg19UCSC Ensembl
Outerchr10:72536112..72554075hg18UCSC Ensembl
Outerchr10:72536112..72554075hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3817964
hg1917964
hg1817964
hg1717964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7077
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)nssv8810
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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