A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7581



Internal ID15552605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122569936..122639333hg38UCSC Ensembl
Outerchr10:124329452..124398849hg19UCSC Ensembl
Outerchr10:124319442..124388839hg18UCSC Ensembl
Outerchr10:124319442..124388839hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3869398
hg1969398
hg1869398
hg1769398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9808, nssv10782, nssv1912, nssv3903, nssv967, nssv6422, nssv11244, nssv9263, nssv10781
SamplesNA18507, NA12156, NA12878, NA18956, NA15510, NA18555, NA18517, NA19240
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)nsv7581
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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