A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2574



Internal ID15540543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:19756250..19775290hg38UCSC Ensembl
Outerchr6:19756481..19775521hg19UCSC Ensembl
Outerchr6:19864460..19883500hg18UCSC Ensembl
Outerchr6:19864460..19883500hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3819041
hg1919041
hg1819041
hg1719041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5219
Supporting Variants
SamplesNA18555
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)nssv2574
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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