A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6878



Internal ID15536985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:146102802..146133465hg38UCSC Ensembl
Outerchr2:146860370..146891033hg19UCSC Ensembl
Outerchr2:146576840..146607503hg18UCSC Ensembl
Outerchr2:146694102..146724765hg17UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3830664
hg1930664
hg1830664
hg1730664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2960
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)nssv6878
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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