A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6422



Internal ID15537442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122569936..122599544hg38UCSC Ensembl
Outerchr10:124329452..124359060hg19UCSC Ensembl
Outerchr10:124319442..124349050hg18UCSC Ensembl
Outerchr10:124319442..124349050hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3829609
hg1929609
hg1829609
hg1729609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7581
Supporting Variants
SamplesNA12156
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)nssv6422
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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