A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7482



Internal ID15205810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:86910566..86941843hg38UCSC Ensembl
Outerchr10:88670323..88701600hg19UCSC Ensembl
Outerchr10:88660303..88691580hg18UCSC Ensembl
Outerchr10:88660303..88691580hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg388162
hg198162
hg188162
hg178162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6405
SamplesNA12156
Known GenesBMPR1A, MMRN2
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)nsv7482
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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