A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5377



Internal ID15550180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:83996429..84031938hg38UCSC Ensembl
Outerchr6:84706148..84741657hg19UCSC Ensembl
Outerchr6:84762867..84798376hg18UCSC Ensembl
Outerchr6:84762867..84798376hg17UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg3835510
hg1935510
hg1835510
hg1735510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4929
SamplesNA19129
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)nsv5377
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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