A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7531



Internal ID15205864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:103858406..103903698hg38UCSC Ensembl
Outerchr10:105618164..105663456hg19UCSC Ensembl
Outerchr10:105608154..105653446hg18UCSC Ensembl
Outerchr10:105608154..105653446hg17UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3845293
hg1945293
hg1845293
hg1745293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5312, nssv8839
SamplesNA12156, NA19129
Known GenesOBFC1
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)nsv7531
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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