A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6856



Internal ID15537007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:88950663..89025952hg38UCSC Ensembl
Outerchr2:89250181..89325449hg19UCSC Ensembl
Outerchr2:89031296..89106564hg18UCSC Ensembl
Outerchr2:89089443..89164711hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3875290
hg1975269
hg1875269
hg1775269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2824
Supporting Variants
SamplesNA12156
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)nssv6856
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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