A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4434



Internal ID15539161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:88859614..88907267hg38UCSC Ensembl
Outerchr2:89159126..89206783hg19UCSC Ensembl
Outerchr2:88940241..88987898hg18UCSC Ensembl
Outerchr2:88998388..89046045hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3847654
hg1947658
hg1847658
hg1747658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2824
Supporting Variants
SamplesNA12878
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)nssv4434
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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