A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543



Internal ID15204777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46278445..46310106hg38UCSC Ensembl
Outerchr10:47649681..47681342hg19UCSC Ensembl
Outerchr10:47119687..47151348hg18UCSC Ensembl
Outerchr10:47119687..47151348hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg385880
hg195880
hg185880
hg175880
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8664, nssv901
SamplesNA12156, NA19240
Known GenesANTXRL
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)nsv6543
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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