A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565



Internal ID15551487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:48152763..48186935hg38UCSC Ensembl
Outerchr10:49360806..49394978hg19UCSC Ensembl
Outerchr10:49030812..49064984hg18UCSC Ensembl
Outerchr10:49030812..49064984hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg385265
hg195265
hg185265
hg175265
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8676
SamplesNA12156
Known GenesFRMPD2, FRMPD2P1
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)nsv6565
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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