A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6067



Internal ID15537796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:54970173..54990931hg38UCSC Ensembl
Outerchr6:54834971..54855729hg19UCSC Ensembl
Outerchr6:54942930..54963688hg18UCSC Ensembl
Outerchr6:54942930..54963688hg17UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3820759
hg1920759
hg1820759
hg1720759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5309
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)nssv6067
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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