A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5731



Internal ID15550570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:7334293..7346090hg38UCSC Ensembl
Outerchr10:7376255..7388052hg19UCSC Ensembl
Outerchr10:7416261..7428058hg18UCSC Ensembl
Outerchr10:7416261..7428058hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385870
hg195870
hg185870
hg175870
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2826
SamplesNA18555
Known GenesSFMBT2
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)nsv5731
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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