A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3871



Internal ID15191912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:33242595..33273182hg38UCSC Ensembl
Outerchr10:33531523..33562110hg19UCSC Ensembl
Outerchr10:33571529..33602116hg18UCSC Ensembl
Outerchr10:33571529..33602116hg17UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg389161
hg199161
hg189161
hg179161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6299
Supporting Variants
SamplesNA12878
Known GenesNRP1
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)nssv3871
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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