A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9808



Internal ID15539869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122587119..122630128hg38UCSC Ensembl
Outerchr10:124346635..124389644hg19UCSC Ensembl
Outerchr10:124336625..124379634hg18UCSC Ensembl
Outerchr10:124336625..124379634hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3843010
hg1943010
hg1843010
hg1743010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7581
Supporting Variants
SamplesNA18507
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)nssv9808
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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