A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6998



Internal ID15536866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:26383651..26411271hg38UCSC Ensembl
Outerchr3:26425142..26452762hg19UCSC Ensembl
Outerchr3:26400146..26427766hg18UCSC Ensembl
Outerchr3:26400146..26427766hg17UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3827621
hg1927621
hg1827621
hg1727621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3741
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)nssv6998
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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