A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2619



Internal ID15200496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:15795223..15829895hg38UCSC Ensembl
Outerchr2:15935347..15970019hg19UCSC Ensembl
Outerchr2:15852798..15887470hg18UCSC Ensembl
Outerchr2:15885945..15920617hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg385355
hg195355
hg185355
hg175355
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3010
SamplesNA18555
Known Genes
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)nsv2619
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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