A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv534



Internal ID15544657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:26339948..26361303hg38UCSC Ensembl
Outerchr6:26340176..26361531hg19UCSC Ensembl
Outerchr6:26448155..26469510hg18UCSC Ensembl
Outerchr6:26448155..26469510hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3821356
hg1921356
hg1821356
hg1721356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5230
Supporting Variants
SamplesNA19240
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)nssv534
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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