A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3164



Internal ID15201060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:218156204..218187521hg38UCSC Ensembl
Outerchr2:219020927..219052244hg19UCSC Ensembl
Outerchr2:218729172..218760489hg18UCSC Ensembl
Outerchr2:218846433..218877750hg17UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg388570
hg198570
hg188570
hg178570
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11029
SamplesNA15510
Known GenesCXCR1
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)nsv3164
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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