A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4085



Internal ID15548759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:159822105..159856177hg38UCSC Ensembl
Outerchr3:159539894..159573966hg19UCSC Ensembl
Outerchr3:161022588..161056660hg18UCSC Ensembl
Outerchr3:161022596..161056668hg17UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg385364
hg195364
hg185364
hg175364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7888
SamplesNA12156
Known GenesIQCJ-SCHIP1, SCHIP1
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)nsv4085
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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