A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6886



Internal ID15536977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:172313484..172335156hg38UCSC Ensembl
Outerchr2:173178212..173199884hg19UCSC Ensembl
Outerchr2:172886458..172908130hg18UCSC Ensembl
Outerchr2:173003719..173025391hg17UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3821673
hg1921673
hg1821673
hg1721673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3034
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)nssv6886
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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